Fungicidal composition (modifications)
专利摘要:
1. I distinguish between a fungicidal agent in the form of an emulsifiable concentrate containing the active substance based on the alanine derivative and the surfactant. y weight in order to enhance the fungicidal activity, it contains a methyl ester of N - 公开号:SU1060095A3 申请号:SU803008192 申请日:1980-11-25 公开日:1983-12-07 发明作者:Рентцеа Костин;Це Бернд;Поммер Эрнст-Гейнрих 申请人:Басф Аг (Фирма); IPC主号:
专利说明:
The invention relates to chemical pest control agents, namely, to a fungicidal agent based on an alanine derivative (its variants). A fungicidal agent is known, containing as active substance a compound of the general formula „„ jf SOI where X is halogen, V is hydrogen, halogen l. A fungicidal agent in the form of an emulsifiable concentrate is known, containing as an active substance methyl K-F (2-furancarbnyl) -M- (2, 6-dimethylphenyl) -alanine methyl FIR and auxiliary cokshon-surfactant and stabilizer I. However, the activity of this means is insufficient. The purpose of the invention is the enhancement of fungicidal activity. This goal is achieved by a fungal agent in its variant solutions. 1. A fungicidal agent in the form of an emulsifiable concentrate, containing, as a derivative, alanine methyl EFIR M - (2-furancarbonyl) -I- (2-methyl 4-bromo-naphthyl) -alany of the formula - c H $. J “H-COOH HIV. . , as a surfactant, sodium ligninsulfonate in the following ratio of components, May. %: Methyl ester of H- {2-furancarbonyl) -N - (2-k: ethyl-4-bromo 1-naphthyl) apanine Sodium ligninsulfonate. -20 2 Fungicidal agent in the form of an emulsifiable concentrate containing N-(3-isoxazolcarbonyl) -M- (2-methyl-1-naphvil) -alanine methyl ester as the derivative, adanine methyl ester, "as a surfactant - the active substance is sodium salt of diisobutylnaphthalene-y-sulfonic acid and sodium ligninsulfonate, and as a stabilizer is silica gel in the following ratio of components, May. %: Methyl ester f4 - (3-isoxazolecarbonyl) -N - (2-methylTN. NaFtil) -alanine 80 Sodium salt of diisobutyl naphthalene-s-sulfonic acid 3 Sodium ligninsulfonate 10 Silica silicic acid 7 Compounds of Formula (I) are obtained as follows the image. 22f2 g (0.066 mol) of K- (2-furancarbonyl) -N- (2-ciutyl-l-naphthyl) -alanine methyl ester and 6 g (0.07 mol) of water-free sodium acetate in 150 ml of acetic acid are mixed with 11 g (0.067 mol) of bromine and stirred for 24 hours at. The mixture is then mixed into 700 ml of ice water, the product is extracted 3 times with 100 ml of ether. The purified ether extracts are washed once with 100 ml of IN sodium hydroxide solution and once with water, dried and concentrated. 17 g (62% of theory) of N - (2-furancarbonyl) -N- (2-methyl-4-bromo-naphthyl) -alanine methyl ester are obtained in the form of a colorless gum. . IR spectrum (film) (cm); 3035, 2930, 1730, 1640, 1450, 1360, 1235, 1190j 1126, 1092, 908.810. Similarly, compound (C) is obtained in the form of a resin, characterized by the IR spectrum (film) (cM ): 3108, 3038, 2935, 1726, 1635, 1532, 14 .., 1330, 1200, 1100, 1042, 875, 856, 810, 796, 778, 758, 742. Comparative compound A was used as a comparison. , cn, cn, cn-coaxial 1-W-CH 3 PRI me R 1, Leaves grown in pots of wheat germ varieties Yubil p are sprayed with an aqueous formulation of a fungicide consisting of, May. %: 80 active substance 1 (test o) or active substance A (experiment 5) and 20 sodium ligninsulfonate. After vyshani, the leaves are pollinated with conidium (s) of powdery mildew of wheat (Erysiphe graminls var. Tritici). Experimental plants are then placed in a greenhouse at a temperature of 2 ° C-22 ° C and relative humidity of 75-80%. After 10 days, the degree of development of the powdery mildew fungi is determined. The results of the experiments are given in the table. PRI me R 2 Leaf ingrown in pots roskov wheat varieties Jubile p is sprayed with an aqueous formulation of a fungicide consisting of, by weight, 80% active substance II (experiment a) , or the active substance A (experiment b), 3 sodium salt of diisobutylnaphthalene-g «b-sulfonic acid, 10 ligninsulfonate. Sodium and 1 Gel of Silicic Acid 1 experience q, famous experience S offered 2 Experiences (Famous run 5, proposed by Crntrol (unprocessed) ; O means no lesion; 100 - complete defeat. . (Eryslphe qramtale var, tritt .. ShG). Experimental plants then becoming Y, in a greenhouse at a temperature; H relative air humidity of 75-80%. After 10 days, the degree of development of the fungal dew fungi is determined. The results of the experiment are given in the table. Percentage lesion fungi leaf. After 10 days with a concentration of the active substance, equal to 0.025% ABOUT 80 35 80 90 Thus, the proposed fungicidal agent has a high activity.
权利要求:
Claims (2) [1] , 1. A fungicidal agent in the form of an emulsifiable concentrate containing an active substance based on A derivative of alanine and a surfactant, I distinguish. more with the fact that, in order to strengthen. fungicidal activity, it contains N - (2-furancarbonyl) i -I- (2-methyl-4-bromo-1'-naphthyl) -alani methyl ester as an alanine derivative. on the formula for the following ratio of components, May. %: N- (2> -furancarbonyl) -N- (2-methyl-4-bromo-1-naphthyl) -alanine methyl ester Sodium Ligninsulfonate [2] 2. A fungicidal agent in the form of an emulsifiable concentrate containing an active substance based on an alanine derivative, a surfactant and a stabilizer, characterized in that, in order to enhance the fungicidal activity, it contains N- (3- isoxazolecarbonyl) -N- (g'-methyl ^ -naphthyl) -alanine of the formula CH 3 I 3 ch-coochj) and as a surfactant sodium ligninsulfonate at the substances are sodium salt of diisobutylnaphthalene-L-sulfonic acid and sodium ligninsulfonate, and as a stabilizer, silica gel in the following ratio, May. ; , N- (3 • -isoxazolecarbonyl-Ν- (2-methyl-1'-naphthyl) -5- alanine methyl ester Sodium salt of diisobutyl- 1 naphthalene — ct — sulfonic acid Sodium ligninsulfonate Silicic acid gel as a surfactant. component
类似技术:
公开号 | 公开日 | 专利标题 RU1837763C|1993-08-30|Herbicidal composition SU1060095A3|1983-12-07|Fungicidal composition | US3546813A|1970-12-15|Fungicidal compositions SU795436A3|1981-01-07|Fungicide composition US5175353A|1992-12-29|2-|-ethanol salt of dicamba ES8301945A1|1982-12-16|Pyridine and pyrazine derivatives, preparation of these compounds, fungicidal agents containing these compounds as active ingredients, and the use of such compounds or agents as fungicides in agriculture and in horticulture. US4266962A|1981-05-12|Drift reducing agricultural compositions IE36337L|1972-11-12|Pharmaceutical compositions US3899585A|1975-08-12|Fungicidal method for protecting a plant EP0566175A2|1993-10-20|3,4-Diaryl |-furan-2-one based compounds with fungicide activity RU2049782C1|1995-12-10|Thiazole derivatives, method of their synthesis, method of struggle against fungi SU655280A3|1979-03-30|Fungicide ES8305357A1|1983-04-16|1,3-Dioxolane derivatives, their preparation, fungicidal agents containing those compounds as active agents and use of such compounds or agents in combating fungi in agriculture and in gardening. US3821403A|1974-06-28|Method of combatting bacteria or fungi on plants using amino acid higher alkyl esters US4567277A|1986-01-28|Salts of 2-|-benzimidazole US2875126A|1959-02-24|New esters of 5-acyl-8-hydroxyquinolines and their use for the control of fungi US4087543A|1978-05-02|Composition for disinfecting soil and combating plant diseases containing organic dicarbonates PT91112B|1995-05-04|PROCESS FOR THE PREPARATION OF PESTICIDE COMPOSITION, FUNGICIDE AND / OR MICROBICIDE, CONTAINING DERIVATIVES OF 4-HALOGEN-5-NITROTIAZOLE AND INTERMEDIATE COMPOUNDS SU1243624A3|1986-07-07|Method of producing derivatives of 3-|-furan US4137332A|1979-01-30|1-|-5-|biguanide compositions for use as agricultural fungicides US3180791A|1965-04-27|Method of controlling fungi with organic sulfur ester compounds JPS63313770A|1988-12-21|Isatin derivative and herbicide containing the same as an active ingredient US4024269A|1977-05-17|Benzimidazole derivatives and fungicidal composition and method US4180569A|1979-12-25|Seed treatment fungicides for control of seed-borne diseases CH635313A5|1983-03-31|PLANT MICROBICIDAL HYDRAZINO ACETANILIDE DERIVATIVES, METHOD FOR THE PRODUCTION THEREOF AND MICROBICIDES WITH THESE PREPARATIONS AS ACTIVE SUBSTANCES.
同族专利:
公开号 | 公开日 CS215143B2|1982-07-30| JPS5692851A|1981-07-27| AU6503180A|1981-06-11| BR8007690A|1981-06-09| IL61515A|1984-02-29| AT2510T|1983-03-15| PL123432B2|1982-10-30| US4430336A|1984-02-07| IL61515D0|1980-12-31| NZ195740A|1982-12-07| EP0029996A1|1981-06-10| MA19006A1|1981-07-01| DK515180A|1981-06-05| EP0029996B1|1983-02-16| ZA807539B|1981-12-30| IE802514L|1981-06-04| DE2948704A1|1981-06-11| HU185622B|1985-03-28| CA1153002A|1983-08-30| IE50726B1|1986-06-25| PL228213A2|1981-08-07| DE3062078D1|1983-03-24|
引用文献:
公开号 | 申请日 | 公开日 | 申请人 | 专利标题 US2412510A|1944-06-02|1946-12-10|American Chem Paint Co|Methods and compositions for killing weeds| DE1003221B|1953-06-24|1957-02-28|Cassella Farbwerke Mainkur Ag|Process for the production of new anesthetically acting aminocarboxamides| NL93512C|1957-04-06|1960-02-15| US3272844A|1965-06-03|1966-09-13|Lilly Co Eli|Novel acetylenic amides| DE1670172C3|1966-12-09|1974-04-04|C.H. Boehringer Sohn, 6507 Ingelheim|2- isoxazolidine| US3549704A|1967-05-19|1970-12-22|Philips Corp|Salicylamides| NL7402417A|1973-03-01|1974-09-03| US4098895A|1975-09-30|1978-07-04|Ciba-Geigy Corporation|Triazolylacetanilide compounds and microbicidal compositions| DE2845454A1|1977-11-01|1979-05-10|Chevron Res|3- - GAMMA -BUTYROLACTONE AND - GAMMA -BUTYROTHIOLACTONE AND FUNGICIDE AGENTS| US4221584A|1979-02-09|1980-09-09|Chevron Research Company|Herbicidal and plant-growth-regulating N--methylacetanilides| MA18800A1|1979-04-10|1980-12-31|Ciba Geigy Ag|ACYLATED NAPHTYLAMINES, PROCESS FOR THEIR PREPARATION AND THEIR APPLICATION AS PHYTOFUNGICIDES|MA19215A1|1980-07-25|1982-04-01|Ciba Geigy Ag|NOVEL ARYLAMINE DERIVATIVES, PROCESS FOR THEIR MANUFACTURE AND USE AS MICROBICIDES.| DE3126083A1|1981-07-02|1983-01-20|Basf Ag, 6700 Ludwigshafen|N-SUBSTITUTED 2-METHYLNAPHTHYLAMID, METHOD FOR THE PRODUCTION THEREOF AND FUNGICIDES CONTAINING THEM| DE3126082A1|1981-07-02|1983-01-20|Basf Ag, 6700 Ludwigshafen|GLYCOLETHERIC ACID APHTHYLAMIDS, METHOD FOR THE PRODUCTION THEREOF AND FUNGICIDES CONTAINING THEM| DE3135239A1|1981-09-05|1983-03-17|Basf Ag, 6700 Ludwigshafen|N-SUBSTITUTED PETROLEUM ACID AMIDES, METHOD FOR THE PRODUCTION THEREOF AND FUNGICIDES CONTAINING THEM| DE3135238A1|1981-09-05|1983-03-17|Basf Ag, 6700 Ludwigshafen|N-ALKINYL-NAPHTHYLAMIDES, METHOD FOR THE PRODUCTION THEREOF AND FUNGICIDES CONTAINING THEM| DE3135670A1|1981-09-09|1983-03-24|Basf Ag, 6700 Ludwigshafen|OXALAMID, METHOD FOR THE PRODUCTION THEREOF AND FUNGICIDES CONTAINING THE SAME| DE3144140A1|1981-11-06|1983-05-19|Basf Ag, 6700 Ludwigshafen|2-ISOXAZOLINE CARBONIC ACID AMIDES, METHOD FOR THE PRODUCTION THEREOF AND FUNGICIDES CONTAINING THEM| DE3144951A1|1981-11-12|1983-05-19|Basf Ag, 6700 Ludwigshafen|ISOXAZOLE-CARBONIC ACID AMIDES, THEIR PRODUCTION AND THEIR USE AS FUNGICIDES| JPH0613445B2|1985-09-10|1994-02-23|保土谷化学工業株式会社|Paddy seed dressing agent| AU4225700A|1999-04-12|2000-11-14|Dow Agrosciences Llc|Aqueous dispersions of agricultural chemicals| RU2646058C1|2017-07-06|2018-03-01|Ксения Леонидовна Алексеева|Method of greenhouses protection from tomato powdery mildew|
法律状态:
优先权:
[返回顶部]
申请号 | 申请日 | 专利标题 DE19792948704|DE2948704A1|1979-12-04|1979-12-04|N-SUBSTITUTED 2-METHYLNAPHTHYLAMID, METHOD FOR THE PRODUCTION THEREOF AND FUNGICIDES CONTAINING THEM| 相关专利
Sulfonates, polymers, resist compositions and patterning process
Washing machine
Washing machine
Device for fixture finishing and tension adjusting of membrane
Structure for Equipping Band in a Plane Cathode Ray Tube
Process for preparation of 7 alpha-carboxyl 9, 11-epoxy steroids and intermediates useful therein an
国家/地区
|