• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:

    公开号:SU1788881A3
    申请号:SU884356228
    申请日:1988-07-22
    公开日:1993-01-15
    发明作者:Takeo Motegi；Mitsumasa Yamazaki；Khiroyuki Iguti；Kaoru Kasakhara
    申请人:Hodogaya Chemical Co Ltd；
    IPC主号:
    专利说明:

    The invention relates to methods including the effect of biologically active substances on the growth and development of cultivated plants, and can be used in agriculture.
    The purpose of the invention is to increase the retardant effect,
    Table 1 shows examples of compounds of this invention. Further, the compounds will be indicated in accordance with the numbering of the compounds in the table. 1.
    Benzamide derivatives according to this invention can be easily obtained in good yields by reacting 4-hydroxy (2,3-dichlorophenyl) benzamide with various esters or amides of haloacetic acid in an organic solvent such as acetone, toluene, dioxane or Ν, Ν-dimethylformamide in the presence of an inorganic base such as potassium or sodium carbonate; or an organic base such as pyridine or triethylamine.
    In addition, they can be prepared by reacting 4-hydroxy- (2,3-dichlorophenyl) benzamide with haloacetic acid in aqueous solution in the presence of an inorganic base such as sodium or potassium hydroxide to give 4- (2,3-dichlorophenylcarbamoyl) phenoxyacetic acid ( compound No. 1) with the introduction of this compound into a reaction with an inorganic acid halide, for example, with thionyl chloride or an organic acid halide such as phosgene in an organic solvent such as dioxane or toluene with conversion into an acid chloride derivative, followed by the introduction of this acid halide into a reaction with various alcohols, alkoxy , alkoxyalkoxy alcohols, alkenyl alcohols, alkenyl alkoxy alcohols, alkynyl alcohols, alkynyl alkoxy alcohols, monoalkyl amines or dialkyl amines in an aqueous solution or organic solvent such as acetone, toluene or
    1788881 AZ dioxane in the presence of an inorganic base such as potassium or sodium carbonate or an organic base such as pyridine or triethylamine.
    PRI me R 1 (obtaining compounds 1+ 2 according to table, 1).
    28.2 g of 4-hydroxy-M- (2,3-dichlorophenyl) benzamide, 20.0 g of ethyl bromoacetate and 20.7 g of potassium carbonate are dispersed in 150 ml of Ν, Ν-dimethylformamide and the dispersion is stirred for 4 hours at 120-140 ° C After completion of the reaction, the reaction solution is poured into 500 ml of 2% HCI aqueous solution. The crude product obtained by collecting the precipitate by filtration is recrystallized from toluene to give 34.5 g of the title 4- (2,3-dichlorophenylcarbamoyl) phenoxyacetic acid ethyl ester. Yield: 93.4%, melting point: 126-129 ° C.
    PRI me R 2 (obtaining compound No. 1 according to table. 1).
    2.82 g of 4-hydroxy-I- (2.3-dichlorophenyl) benzamide and 1.67 g of bromoacetic acid are dissolved in 10 ml of dioxane. To this solution, a mixture of 0.97 g of sodium hydroxide and 2 ml of water is added dropwise over 10 minutes with stirring and a temperature of 20 ° C. After the addition, the reaction mixture was stirred for 2 hours at 80 ° C. After completion of the reaction, the reaction solution is poured into 50 ml of water and acidified with hydrochloric acid. The crude product is collected as a precipitate by filtration, recrystallized from toluene / methanol to give 2.5 g of the desired 4- (2,3-dichlorophenylcarbamoyl) phenoxyacetic acid.
    Yield: 70.6%, melting point: 198-199.5 ° C.
    Primerz (preparation of compound No. 5 according to Table 1).
    A mixture of 3.54 g of 4- (2,3-dichlorophenylcarbamoyl) phenoxyacetic acid, 3.57 g of thionyl chloride and 30 ml of dioxane is stirred for 4 hours at 80 ° C. Excess thionyl chloride and dissolved HCI gases. sulfurous acid and dioxane are distilled off on a rotary evaporator to give 4- (2,3-dichlorophenylcarbamoyl) phenoxyacetyl chloride as a distillation residue.
    0.8 g of n-butanol and 2.0 g of triethylamine are dissolved in 20 ml of dioxane. To this solution, a solution of the 4 (2,3-dichlorophenylcarbamoyl) phenoxyacetyl chloride obtained above in 5 ml of dioxane is added dropwise over 5 minutes at room temperature with stirring. After completion of the dropwise addition, stirring is continued for an additional 5 hours at room temperature. After completion of the reaction, the reaction solution is poured into
    200 ml of 2% HCI aqueous solution. The precipitate is collected by filtration, washed with dilute aqueous alkaline solution and water, and then dried. Then the residue is recrystallized from toluene and 3.3 g of 4- (2,3-dichlorophenylcarbamoyl) phenoxyacetate n-butyl ester are obtained. Yield: 80.5% based on 4- (2,3-dichlorophenyl) carbamoylacetic acid, melting point: 132-136 ° C.
    PRI me R 4 (obtaining compound No. 18 according to table. 1).
    0.71 g of isopropylamine and 3.0 g of triethylamine are dissolved in 20 ml of dioxane. To this solution, a solution prepared by dissolving 4- (2,3-dichlorophenylcarbamoyl) phenoxyacetyl chloride is added dropwise with stirring at room temperature over about 5 minutes. obtained in example 3, in 5 ml of dioxane. After completion of the dropwise addition, stirring is continued at room temperature for an additional 5 hours. After completion of the reaction, the reaction solution was treated as in Example 3 to obtain 3.8 g of the target 1M-isopropyl-4 (2,3-dichlorophenylcarbamoyl) phenoxyacetamide. Yield: 92.5% based on 4- (2.3 dichlorophenylcarbamoyl) phenoxyacetic acid, melting point: 159-161.5 ° C.
    PRI me R 5 (obtaining compounds Ns 30 according to table. 1).
    1.02 g of 4- (2,3-dichlorophenylcarbamoyl) phenoxyacetic acid are dissolved in 5 ml of methanol. To this solution, 0.33 g of triethylamine is added dropwise, with stirring at room temperature, over about 5 minutes. Stirring is then continued for 1 hour at room temperature. Then the excess of triethylamine and methanol is distilled off on a rotary evaporator to obtain 1.2 g of the target salt of triethylamine and 4- (2,3-dichlorophenylcarbamoyl) phenoxyacetic acid. Yield: 90.7%, melting point: 153 ~ 157 ° C (decomposition).
    The plant growth regulator according to this invention can be obtained, for example, in the form of a wettable powder, emulsifiable concentrate, liquid formulation, granules, dust, flowable or aqueous solution by mixing the active ingredient with carriers of various types depending on their physicochemical properties.
    Among carriers such as liquid carriers, conventional organic solvents can be used, and as solid carriers, conventional mineral powders can be used. In addition, when making such a formulation, a surfactant to improve emulsifiability, dispersible ™ or spray ™ formulation can be added. In addition, if necessary, the compound of this invention can be combined with a fertilizer, herbicide, insecticide or fungicide in the form of a ready-made formulation or tank mix for application.
    An inorganic compound such as bentonite, clay, zeolite or talc can be used as a carrier. As the organic solvent, a solvent in which various compounds are readily soluble, for example xylene, toluene, cyclohexanone or glycol, can be used. In addition, anionic or nonionic surfactants such as lignin sulfonate, naphthalene sulfonate, dialkyl sulfosuccinate, polyoxyethylene nonyl phenyl ether, polyoxyethylene stearyl ether or polyoxyethylene dodecyl ether can be used as dispersing, emulsifying or fixing agents.
    When a compound of this invention is used as a herbicide, the active ingredient is applied in an amount sufficient to achieve the desired herbicidal effect. The dose of the active ingredient is in the range of 1-200 g / are. usually preferably 5-50 g / are. It can be formulated such as a wettable powder, emulsifiable concentrate, dust or granules, which contain the active ingredient in an amount of 0.1-80 wt%, preferably 1-50 wt%.
    When the compound of the present invention is used as a herbicide, it basically suppresses the emergence and growth of weeds, gradually kills the weeds. In flooded fields, the herbicide of the present invention exhibits excellent herbicidal action against not only annual weeds such as millet, but also perennial weeds such as arrowhead and fan-shaped weeds. No phytotoxicity was noted against the transplanted rice plants. In addition, when applied to soil or foliage on dry land, it exhibits a selective herbicidal effect on maize, soybeans and the like.
    When a compound of this invention is used as a plant growth regulator, it can be applied at a dosage of active ingredient in the range of 1-10 g / are depending on the type of plant, the type of compound or the time of application. The active ingredient can be formulated such as wettable powder, emulsifiable concentrate, dust or granules, which contain 0.1-80% by weight, preferably 1-50% by weight, of the active ingredient.
    As a specific effect on cereal plants, a decrease in the distances between nodes after treatment and is observed. in some cases, stimulation of shoot formation. In the case of broadleaf plants, the plant growth regulator of the present invention effectively inhibits new bud formation, prevents longitudinal growth, or promotes axillary bud or flower bud formation.
    Thus, the compound of this invention has a wide variety of uses, for example, as a lodging reducing agent, as a restrictive pruning agent, as a shortening agent for flowering trees, grasses or large weeds, or as a thinning agent.
    If the compound of this invention is used as a plant growth regulator and is applied to foliage, the dose will vary depending on the type of plant and the purpose of the application.For example, if it is used to reduce lodging of plants, it can be applied at a dose of 0.5-3 g / are in the case of rice and 2-10 g / are in the case of wheat. If used to shorten a plant, it can be used in an amount of 3-15 g / are in the case of herbs such as Bermuda herb.
    Below are examples of possible recipes.
    Getting a wettable powder.
    Up to 40 wt. parts of compound No. 5 are added 52 parts by weight of kaolin and 3 parts by weight of silica, and the mixture is mixed and ground in a mixer. Then 4 parts of powdery surfactant Sorpol 5039 and 1 part by weight of powdery surfactant Rapizol B B-75 are mixed to give a wettable powder containing 40 weight% of compound No. 5.
    Obtaining an emulsifiable concentrate.
    parts by weight of compound No. 10 are dissolved in 42 parts by weight of xylene and 33 parts by weight of cyclohexanone, 10 parts by weight of Sorpol 800A are added. dissolving is carried out with stirring and an emulsifiable concentrate is obtained containing 15 wt.% of compound No. 10.
    Getting dust!
    By 50 wt. parts of compound No. 1 are mixed with 3 parts by weight of carbon black and 47 parts by weight. parts of kaolin clay and the mixture is ground. Two parts by weight of the milled mixture are added to 96 parts by weight of the finely divided zeolite with stirring in a high speed mixer. While stirring, 2 parts by weight of polyoxyethylene dodecyl ether diluted with water are added. The mixture is prepared by adding a small amount of water until the powder disappears. The mixture was taken out, dried in a stream of air and received a microgranular formulation containing 1 wt.% Of compound No. 1.
    To 50 parts by weight of the compound GF 3 are added 3 parts by weight of carbon black and 47 parts by weight of clay, and the mixture is ground in a mixer. The mixer is charged with 2 parts by weight of the crushed 15 mixture, 40 parts by weight of bentonite, 43 parts by weight of clay, 5 parts by weight of sodium tripolyphosphate and 2 parts by weight of powdered surfactant Rapizol BB-75 (trade name), and the mixture mix thoroughly. Then water is added, the mixture is thoroughly mixed, granulated on a granulator, dried in a stream of air and granules are obtained containing 5 wt% of the compound GF 3. 25
    PRI me R 6 Test by treating the leaves of various plants (plant growth regulator). ,
    Rice, barley, kidney beans and lettuce are independently grown in 80 cm 2 porous pots and thinned according to the size of the plants. The plants are grown to the 2-3 leaf stage and a dilute solution of each test compound 35 is sprayed onto the foliage at 10 L / are. Growth inhibition is assessed on day 30 after treatment. The results are presented in table. 2.
    The assessment is carried out on the following scale:
    Height inhibition. 40
    0: the same as without processing.
    1: Inhibition of about 20% compared to untreated control.
    2: Inhibition of about 40% compared to untreated control, 45
    3: Inhibition of about 60% compared to untreated control.
    4: Inhibition of about 80% compared to untreated control.
    5: No further growth of 50 is observed after treatment.
    Processing effect.
    C: Enhanced green color.
    T: Formation of shoots.
    M: The ugliness of the leaves. 55
    Q: Swelling. blackening of foliage,
    PRI me R 7. Test processing of azalea leaves.
    A diluted solution of each test compound is applied to azalea seedlings (height 25-30 cm), growing in porous pots with an area of 200 cm 2 , until all seedlings are completely wetted (25 l / are). After 7 days, they are trimmed and after 2 months the evaluation is carried out in the same way as in example 6. The results are presented in table. 3.
    Example 8. Reduced lodging in rice.
    The rice field to which the seedlings of the rice plant (Koshikhikari) were transferred for cultivation in such a field by means of a carrier was divided into separate plots of 3 x 6 m in mid-May. 30 days before the formation of ears, 300 g / ar of inabenfid granules were applied manually as a comparison tool. Further, 20 and 6 days before heading, 2 L / ar of a dilute solution of a compound of the present invention is applied by spraying with a hand sprayer.
    After 4 weeks, the stem length and panicle length are measured in 20 plants. 6 weeks later, a rice plant is harvested on a 3 m 2 plot and the grain weight (kg / acre) and 1000 grain weight are measured. Lodging is inspected at appropriate time intervals and evaluated against the following standards:
    Lodging index on the vine.
    0: No lodging on the vine
    1: Weak lodging
    2: Slight lodging
    3: 50% lodging (45 ° tilt.
    50% completely died).
    4: Significant lodging
    5: Full lodging.
    The results are shown in table. 4.
    Numerical values represent percentages relative to the untreated plot.
    The values in parentheses represent the actual measured values.
    PRI me R 9. Reduction of lodging of wheat plants on the vine.
    A field planted with wheat (Katakami) at the end of September in northern Japan is divided into separate plots of 3 x 8 m.With diluted solutions of the compounds of the present invention and the agents used for comparison, this field is sprayed with a dose of 2.5 l / are using a sprayer, operating under pressure (1.5 m hose). Spraying is carried out in accordance with Tsadoks-Ji.ES. GF 32-33 and 41-42. The ears formed at the end of May. Harvested in mid-July
    Research on various indicators is carried out at the end of June. those. a month after the appearance of ears and by the time of harvest.
    The studies were carried out in the same manner as in test example 8. The results are shown in table. five.
    Example 10. Test for processing chrysanthemum foliage (Because).
    According to the usual method, "chrysanthemum" chrysanthemums (host plants) are planted as cuttings at the beginning of August and after 2 weeks are transferred into pots, 200 ml, 5 plants per pot. Further, after 2 weeks, the pot is pinched. Then, after 2 weeks, electric light is irradiated at night for 3 hours, 3 pots (plant height about 5 cm) are used as one combined plot. The compound of the present invention and daminoside are applied by spraying so that the leaves remain sufficiently hydrated (5 ml per pot) and tests are carried out after 1 month and 2 months (at the time of flowering). The results are shown in Table 6. Numerical values represent the percentages relative to the untreated plot. The values in brackets represent the actually measured values.
    Test Example 11. Foliage Treatment Test on Trees.
    A fairly thick section of the branches of each tree is chosen, and when new buds grow up to 3/5 cm, the branches are divided into plots from 1 to 2 m, which are sprayed. Spraying with solutions of these funds is carried out not only from the top, but also from the sides. so that the solutions are carried out on all trees as a whole. The dosage is 8 to 15 l / are.
    After 4 months, the growth of new branches is assessed.
    The results are shown in table. 7.
    The plots accepted for spraying are as follows:
    Types Width, cm Height
    trees trees. cm Rhododendron in dicum 60 70 Buxus microphilla 50 60 Photinia glabra 80 120 Abella serrota 70 70 Juniperus chinmsis 80 140
    The estimated indicators are as follows:
    0: Same as untreated pot
    1: 20% inhibition
    2: 40% inhibition
    3: 60% inhibition
    4: 80% inhibition
    5: Complete inhibition (no growth since treatment).
    Π example 12. Processing the foliage of the Bermuda grass.
    The lawn covered with Bermuda grass (T-419) is divided into 3 unit plots of 4 m 2 each. Before May mowing, spraying with dilute solutions of the compounds of the present invention and mefluidide B-2,4-dimethyl-5- (trifluoromethyl) sulfonylaminophenylacetamide is carried out, respectively, at a dosage of 2 l / are. using a hand sprayer.
    weeks later, research and mowing is carried out (height of the mowed grass 100 mm), and the height of the mowed grass is measured.
    Thereafter, the mowing is stopped and 5 weeks later the evaluation is made in comparison with the untreated plot.
    The results are shown in table. eight.
    Numerical values represent percentages relative to the untreated plot. The numerical values enclosed in brackets () are the actual measured values.
    The evaluation is carried out in the same way as described in example 11. However, the density is evaluated according to the following indicators:
    D-0: normal
    D-1: less density
    D-2: dense
    D-Z: high dense. Phytotoxicity.
    B-1: Weak coloration of foliage.
    B-2: Moderate foliage coloration
    Q-3: Significant coloration of foliage.
    C-1: Slight whitening or yellowing
    C-2: Moderate whitening or yellowing
    C-3: significant whitening or yellowing
    Other responses:
    G-1: Weak green indentation
    G-2: Moderate green indentation
    G-Z: Significant depression in green
    T-1: Weak tillering
    T-2: Moderate tillering
    T-3: Considerable tillering.
    Example 13. Test for thinning apples.
    Among the branches of an apple tree, which is 25 years old, the same branches are selected and 20 days after full flowering, a solution of each compound with a given concentration is sprayed onto whole branches with a sprayer, using a solution in such an amount that the spray applied solution does not drip from the branches. After 2 months, the degree of fruiting and the diameter (distance from one side to the other) of the fruit are assessed. The results are presented in table. nine.
    PRI me R 14. Test of the processing of foliage of sugar cane. five
    After the sugarcane has grown to the primary stage of maturity, it is divided into sections, where each section contains 5 plants, and 30 ml of a solution having a given concentration of active ingredient is applied to the base parts of the upper leaves of each stem using a hand sprayer.
    After 2 months, i.e. by the time of harvest, some heading is observed in the untreated plots, while this is not observed in every treated plot. The plants are harvested and squeezed, and the sugar content of the squeezed juice is measured with a polarimetric 20 sugar meter.
    The results are presented in table. ten.
    PRI me R 15. Test by processing the foliage of soybeans.
    Soybeans (Enrei) are grown in a greenhouse in 200 cm 2 pots (1 plant / pot). At the beginning of the 3-leaf stage, each compound diluted to a predetermined concentration and having 500 ppm added nonionic surfactant is applied in an amount corresponding to 10 L / are. The tests are carried out using 3 plants per plot. After 2 months, the number of pods formed is estimated. The results are presented in table. 11. (Figures represent the average of 3 plants and are rounded to one decimal place).
    权利要求:
    Claims (1)
    [1]
    Claim of the invention A method for regulating the growth of cultivated plants, comprising treating them with a biologically active substance 15, characterized in that, in order to increase the retardant effect, a compound of the general formula is used as a biologically active substance
    CI C1. ^ nhco <o> och 2 cor, where R is hydroxyl. group ON. or ONH (C 2 Hs) 3, or oxyethyl, oxy-n-butyl, 2butoxyoxyethyl. 2-butoxy-2-ethoxyethyl, or monoethylamino group, or dimethylamino group, at a dose of 1-10 g / are.
    Table 1
    Compounds of the invention
    Connection No. Chemical formula Melting point, ° C 1 C1 C1 @ -mnso / o) -asn 2 coon 198-199.5 2 С1 С1 ^ NHC0- <O> -0CH 2 C00C 2 H5 126-129 3 ci ci @ -knso- <o> -osn 2 coos 3 n 7 - p 131-135 4 C1 C1 @ -MHC0- <O> -0CH 2 C00C 3 H 7 -i 130-132 five - Cl Cl ^ -mnso- <o) -base 2 coax ^ n e - η 132-136
    Continuation of table. 1
    Connection No. Chemical formula Melting point, ° C 6 Cl CI^ ynsso- ^ osngsoosfe-cheo 114-118 7 CI C1 ^ ynso // osh 2 coos ch n e -1 149-150.5 eight CI C1 @ -NHC0 - <^> - 0CH 2 C00C 6 H u -h 158-161 nine Cl Cl <^ NHC0X ^ 0CH 2 C00C n H 25 -n 153-158 ten Cl Cl <^ nhco <c / och 2 cooch 2 - 87-92 eleven -ch 2 oc 4 h 3 - η Cl Cl '<@ - shco - @> - main 2 coax 2 sn 2 ~ 65-70 12 -ОСН 2 СН 2 ОЦН 3 -П ci ci ^ NHC0 <^ 0CH 2 C00CH 2 CH = CH 2124-1127 13 Cl Cl ^ NHCO- <0> -OCH 2 COOCH 2 CH = 135-139 fourteen = CHCH 2 CH 3 Cl ci ^ nhco <^ och 2 cooch 2 c = ch 95-101 fifteen Cl C1 ^ inso - <^ osn 2 soknsn 3196-197.5 sixteen Cl Cl ^ nhco <c / och 2 conhc 2 h 5158-160.5
    Continuation of table. Ί
    Compound I + Chemical formula Melting point, ° C 1718 С1 С1 ^ $ - NHC0- (o> -0CH 2 C0NHC 3 H 7 -η Cl 01 ^ NHCO ^ OCH 2 CONHC 3 H 7 -l V, 170-171.5159-161.5 nineteen Cl Cl^ NHCO - ^^ OCfyCONHC ^ Hg-Tl 141-142 20 Cl Cl ^ NHCO <^ OCH 2 CONHC 4 H 3 4SO 170-171 21 Cl Cl <^ NHCOXc ^ OCH 2 CONHC 4 H 9 -t 166-168.5 22 Cl ci ^ NHCoX ^ OCH 2 CONHC 12 H 25 -n 129-131.5 23C L CI 7 n s @ -NHC0- © h OCHjCON < ch136-138 24 C1 d C 2 H 5 ^ NHCO- ^ OCfy CON C 145.5-147 25 ci Cl c H -n ^ -NHC0 - @) - 0CH 2 C0Ni 3 7138-140.5 26C L ' l k s ^ NHC0 - <^ 0CH 2 C0N Xc ^ _ n128-130.5 27 Cl Cl C ^ Hg-n ^ -NHC0 <O> -0CH 2 C0N7 r ^ H ^ n140.5-144
    Continuation of table. 1
    Connection No. Chemical formula Melting point, ° C 28 C1C1 C ^ Hg-Sec @ -NHCO <o / OCH 2 CON x ^ HrSec . 143.5-146 29 Cl Cl ^ -NHCO- © -OCH 2 COONa Above 230More than 230 thirty Cl Cl B $ -INS0LO ^ 0СН 2 С00Н · WC 2 H 5 h 153-157(Decomp.) / Decomposition / 31 Cl ci ^ nhco- <o) -och 2 cooh. B1Н 2 С jH'j ”! ' 203-207(Decomp.) / Part / 32 C1 ci @ -MHC0 - ^> - 0CH 2 C00H. w g s h n e -p 150-154(Decomp.) /Razl./
    table 2
    Evaluation of the inhibitory effect of the compounds of the invention
    Connection No. Concentration,% e reaction of the test plant Rl xVA XFR X1E X 1 0.1 five five 4.5MB five 0.05 4T 5T 4 five 0.025 3 4 4 4 2 0.1 five 4T 5B five 0.05 4T 3 five five 0.025 3.5 3 4 4 4 0.1 4.5T 4T 4.5MV five 0.05 4.5T 4T 4.5M five 0.025 4 3.5 4 4.5 five 0.1 five 4T 4.5M 4 0.05 five 4 4 4 0.025 4T 3 3.5 3 7 0.1 4T 3 4 4 0.05 3 3 3 3 0.025 2 2 2 2 eight 0.1 4 3 4 4 0.05 3 2 4 3.5 0.025 2 1.5 3 2 ten 0.1 4T 4.5T 5MV five 0.05 4T 4T 4.5M five I 0.025 3.5 3.5 4 4.5
    Continuation of table. 2
    Connection No. Concentration,% Test plant response | Rl xVA XΊΊX 1E X I 12 0.1 4.5T 4T 5MV 4 0.05 4.5T 4 4.5 4 0.025 4 3.5 4 3.5 13 0.1 4 3 4 4 0.05 3 3 3 3.5 0.025 2 2 2 2.5 fourteen 0.1 4T 4T 4 3 0.05 4 4 3.5 3 0.025 3 3 3 2 fifteen 0.1 five five 5MV five 0.05 4.5T 4T 4.5M five 0.025 3.5 3 4 4 17 0.1 five 4T 5MV five 0.05 4.5T 4T 4.5 five 0.025 4T 3.5 4 4 nineteen 0.1 five 4T 4 4 0.05 five 4 4 4 0.025 4T 3.5 3 3.5 23 0.1 5T 4 5MV five 0.05 5T 4 4.5 6 0.025 4 3.5 4 4.5 25 0.1 3 3 3 3 0.05 3 2.5 3 2 0.025 2 2 2 1.5 29 0.1 5T 5T Bmw 4 0.05 4 4 4 4 0.025 3 4 4 4 thirty 0.1 five five 5MV 4 0.05 4T 4.5 4.5 4 0.025 3.5 4 4 3.5 The famous 0.1 0 _____0 0 0
    fl Note x R1: Fig
    VA: Barley
    TR: Common beans
    IE: Salad
    Table 3
    Azalea foliage treatment test
    Connection No. Concentration,% Growth inhibition Other effects | 1 0.1 4 G0.05 32 0.1 five GB0.05 4five 0.1 4 M0.05 3ten 0.1 4.5 G0.05 4fifteen 0.1 4 0.05 3.5 '24 0.1 4 G0.05 3
    Continuation of table. 3
    Connection No. Concentration,% Growth inhibition Other effects 29 0.1 4 M 0.05'‘3 thirty 0.1 3.50.05. 3
    Table 4
    Terms of processing Connect Dose After 4 weeks 6 weeks / after harvest ki nenie assets- harvest / leg In- Length Length In- % co- Weight Weightingre- deck stem broomstick deck ripening 1000 grains,diene field-ki field- shih grains kg / arthat. on on grains g / ar root root 6 days before 1 1 0 85 101 0 108 103 108 ears2 0 80 99 0 109 104 109 ev five 1 0 80 93 0 107 104 1082 0 74 100 0 107 103 107 29 1 0 88 98 0 108 102 1072 0 82 101 0 109 104 110 20 days before 1 1 0 93 100 0 112 101 112 development of co-2 0 86 102 0 109 104 110 moose five 1 0 89 98 0 108 103 1082 0 82 99 0 113 101 111 29 1 0 92 103 0 115 102 1142 0 87 98 0 109 104 110 30 days before * Wed- development of co- ntel- moose ny 18 2 96 96 3 103 103 105 No processing 3 100 100 4.5 100 100 100 / 96.8 / 18.5 cm/ / 66.9 / / 22.1 / 54.0 I cm/ g / COP /
    x Inabefid 6% granules 4'-chloro-2 '- /' - oxybenzyl / -isonicotinoylanilide
    Table 5
    Effect of Compounds of the Invention on Wheat Lodging
    Compound Dose of active ingredient, g / ar 4 weeks after ear formation When harvesting Lodging index Stem length at harvest Lodging index on the root / 0-5 / Weight 1000 z-ren Output / kg / ar /2 1 94 2 107 1114 0 87 1 106 109 2 eight 0 81 0 106 110 Z2 1 96 3 105 108 GS sixteen 4 0 87 1 107 115 32-33eight 0 83 0 108 113
    Continuation of table. five
    Compound Dose of active ingredient, g / ar 4 weeks after ear formation When harvesting Lodging index Stem length at harvest Lodging index on the root / 0-5 / Weight 1000 z-ren Output / kg / ar /2 1 92 2 108 110 thirty 4 1 88 1 107 112eight 0 83 0 108 114 sss 12 2 95 3 104 10724 1 93 2 105 109... 2 0 85 0 108 1134 0 79 0 109 112 2 eight 0 73 0 107 1092 0 93 1 109 1114 0 89 0 107 113 Z sixteen eight 0 84 0 106 110 G541-422 1 84 0 108 •1154 0 78 0 108 114 thirty eight 0 73 0 106 108 sss 12 3 98 4 102 10424 2 94 3.5 104 106 Ethephone eight 0 81 0 96 95-100100 100 Inappropriate - 3.5 / 97 / 4.5 /40.6/ /52.8/ nerd- naya.. plot
    Table 6
    Chrysanthemum foliage processing test
    Compound Active ingredient concentration / ppm / After 1 month Height / cm / After 2 months / at the time of flowering / Height / cm / Flower stem / cm / Number of leaves Number of effective flowers The number of delays before flowering 200 70 76 70 100 100 0 4 400 64 70 62 100 100 0 800 55 67 57 ... 106 105 0 200 62 70 66 100 100 0 12 400 55 60 56 106 105 1 800 44 53 49 111 111 2 200 75 78 72 100 100 0 31 -400 67 71 65 100 105 0 800 60 66 59 106 105 about I
    Continuation of table. 6
    Compound Active ingredient concentration / ppm / After 1 month Height / cm / After 2 months / at the time of flowering / Height / cm / Flower stem / cm / Number of leaves Number of effective flowers The number of delays before flowering Diaminoside 4000 72 74 67 100 105 0 Untreated plot100/30.1/ 100 /45.4/ 100 /8.2/ 100 / 18.3 / 100/ 10.8 / 0
    Table 7
    Foliage Treatment Test for Trees
    Types of trees Compound No. 6 Dikegulak-sodium 0.1% 0.2% 0.2% 0.4% Azalea / Rhododendron / 4 4.5 2 3.5 Boxwood / Buxus / 3.5 4.5 1 2 Hawthorn / Photinia / 4 4.5 2 4 Abelia 3 4 0 2 Juniperus 3 4.5 2 2.5
    Table 8
    Test by processing foliage, bermuda grass
    Connection - g / ar 2 weeks later 5 weeks later Growth inhibition Grass weight / g / cm 2 / Other reactions Growth inhibition Other reactions 2.5 4 33 G-1 3 I D-1 1 five 4.5 thirty G-2 4 G-1 D-3 ten five 26 G-2 4.5 G-2 D-3 2.5 4.5 28 G-2 3 ! D-2 2 five five nineteen G-2 4 'G-1 D-3 ten18 G-3 4.5 : g-2 D-3 2.5 4 32 G-2 3.5D-1 eleven five five 25 G-2 4 ; G-1 D-3 ten five 12 G-3 4.5 I G-2 D-1 2.5 4 thirty G-1 3D-3 29 five 4.5 22 G-2 4 G-1 D-3 ten ten five fifteen IN 1 4.5 G-2 D-2 Meflu- 2.5 1 841D-0 BIT five 1 782D-0 ten 2 65 IN 1 3 G-1 D-0 j Inappropriate secret de- lanka0 1000D-0 /42.5/
    Table 9
    Apple Thinning Test
    Connection, no. Concentration / h / min / Number of fruits tested Test results,% of untreated branches Central fruits Side fruit Fruiting degree, '% Average fruit diameter,% of required branches Central fruits Side fruit I 50 39 120 71.8 8.3 111 25 32 101 87.5 9.9 114 12.5 37 113 86.5 11.5 109 II 50 35 108 71.4 7.4 106 25 .37 110 86.5 10.0 112 12.5 thirty 99 90.0 12.1 110 Untreated arearunoff34 102 82.4 27.5 100 (35.9 mm)
    Table 10
    Results of measuring the juice content in sugar cane
    Connection No. Active ingredient,% Average sugar content,% 1 0.2 13.83 0.1 13.57 ten 0.2 14.21 0.1 13.84 29 0.2 12.98 0.1 11.95 Untreated area - 10.39
    Table 11
    Connection No. Active ingredient,% Number of pods I thirty 31.0 100 35.3 300 33.3 II thirty 28.3 100 39,7 300 38.0 29 thirty 25.0 100 35.3 300 37.3 thirty thirty 26.0 100 36.3 300 32,7 Untreated area - 24.7 I
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