Herbicidic agent
专利摘要:
A composition containing at least one compound of the formula <IMAGE> (I) in which R is alkyl, alkenyl, alkinyl, halogenoalkyl or alkoxyalkyl, R1 is alkoxyalkyl or dialkoxyalkyl, R2 is alkyl or alkoxy, and x is oxygen or sulfur and n is 0, 1, 2 or 3. The compounds have a strong herbicidal effect against various weeds together with a broad selectivity in regard to agricultural plants, particularly potatoes, cotton, peanuts, carrots and rice. 公开号:SU717990A3 申请号:SU782632100 申请日:1978-07-03 公开日:1980-02-25 发明作者:Арндт Фридрих;Борошевски Герхард 申请人:Шеринг Аг (Фирма); IPC主号:
专利说明:
(54) HERBICID MEANS ,; - - -.one . ; ; // The invention relates to chemical agents for controlling weeds and undesirable vegetation (ai), namely, to a terbicidal agent containing an active principle from among carbohydrate-carboxylic acid derivatives and auxiliary components from a group of liquid or solid nosyogels, surfactants, etc. A herbicidal agent is known, the active principle of which is E-methoxycarbonylamino-phenyl ester of 3-methylcarbanilic acid and. its analogues 1. The prototype of the invention is herbicidal agents on the axis of carbamic acid derivatives. These include, for example, an agent based on urethanes-3-Calkyloxy-Idyl-alkylthiocarbonylinol-phenyl esters of M-allyl-N-benelikarbamoyoy acid 2 However, the known herbicidal agents of this group are not sufficiently effective for certain types of weeds and are not selective for crops, The aim of the invention is a new Herbicidal agent based on carbamic acid derivatives, possessing a pyuyoy gerbicide effect, activity and selectivity of action. This is achieved by using a carbamic acid derivative of the general formula, 1 - ten NHC-XR a) N-C-O alkyl, 2-methoxyethyl, where R is chloroethyl, bromstil, chloroisopropyl, allyl / propargyl; R - alkoxyzistil C, -C, 2,2-dimethoxyethyl, 2,2-diethoxyethyl; , -methyl or methoxy; - O or 1; P .. - oxygen or sulfur. X The content of the active principle in the herbicidal agent ranges from 1 ° C to 80% by weight. The forms of application of the active substances are ordinary: solutions, emulsions, pastes, powders, etc. They are prepared by known methods. Recommended doses of the active principle for the selective destruction of weed plants range from 0.5 to 5 kg / ha. The method of obtaining compounds of the general formula. based on the reaction of the corresponding aryl chloroformates with N-substituted anilines in the presence of a hydrogen chloride accelerator. They are also prepared by reacting 3-acylaminophenols with N-arylcarbamyl chloride or other known methods. N- (2-methoxyethyl) -car1-carboxylic acid 3- (Мё1 6xycarbonyl mino) -phenyl ester N- (2,2-dimethoxyethyl) -carbanilic acid 3- (methoxycarbonylamino) -phenyl ester 3- (Methoxycarbonylamino) -phenyl ester of N- (2-methoxyethyl) -3-methylcarbanyl acid 3- (Ethoxycarbonylamino) -phenyl ester of N- (2-methoxyethyl) -carbanilic acid 3- (Isopropoxy1 arbonylamino) -phenyl ester of N- (2,2-di-methoxyethyl) -carbanilic acid -. . . ,, ,,,, ..,;,::.,. :: V;, ..., - --- L-- 3- (Isopropoxycarbonylamino) -phenyl ester of N- (2-methoxyethyl) -carbanilic acid Z-Sec - Butoxycarbonylamino-phenyl ether of N- (2-methoxyethyl) -carbanyl acid 3-Isobutylcarbonylamino-phenyl ether N- (2,2-dimethoxyethyl) -carbanyl ACID 3- (2-Methylpropoxycarbonylamino) -phenyl ester of N- (2-methoxyethoxy) -, carbanyl. acids Z- (Allyloxycarbonylamino) -phenyl ester of N- (2-methoxyethyl) -carbanilic acid Z- (Allyloxycarbonylamino) -phenyl ester of N- (2,2-di1 "5 tethoxyethyl) -carbanyl acid 3- (2-Propynyloxycarbonylamino) -phenyl ester of N- (2,2-dimethoxyethyl) -carbanilic acid 3- (2-Propynyloxycarbonylamino) -phenyl ester of N- (2-methoxyethyl) -carbanilic acid - - - 3 (Methylthiocarbonylamino) -phenyl ester of N- (2, 2-dimethoxyethyl) -carbonyl acid 3- (Ethylthiocarbonylamino) -phenyl ester of N- (2,2-dimethoxyethyl; -carbanilic acid 1, Post-emergence Example experience. . Experimental plants grown under greenhouse conditions up to a certain stage of development are treated with preparative forms of the active substances with a preparation consumption rate of 600 l / ha, which corresponds to 5 kg / ha of the active substance. Evaluation of the herbicidal action was carried out after 3 weeks post processing. The results of the experiment are given in table. one. T a faces 4 4 4 4 Z- (Ethylthiocarbonylamino) -phenyl ester of N- (27-methoxyethyl) -carbanilic acid 3- (Methoxycarbonylamino) -phenyl ester of 1Н- (2-ethoxyethyl) -carbanyl acid 3- (Methoxycarbonylamino) -phenyl ester 1SI- (2-ethoxyethyl) -3-methylcarbanilic acid 3- (Methoxycarbonylamino) -phenyl ester of (2,2-dimethoxyethyl) -3-methylcarbanyl acid N- (2,2-dimethoxyethyl) -4-methylcarbanyl 3- (methoxycarbonylamino) -phenyl ether acids 3- (Etoxycarbonylamino) -phenyl ester of N- (2-methoxyethyl) -3-methylcarbanyl acid 3- (Ethoxycarbonylamino) -phenyl ester of N- (2-ethoxyethyl) -carbanilic acid 3- (Ethoxycarbonylamino) -phenyl ester of N- (2,2-dimethoxyethyl) -3-methylcarbanilic acid 3- (Ethoxycarbonylamino) -phenyl ester of N- (2-ethoxyethyl) -3-methylcarbayl acids 3- (Ethoxycarbonylamino) -phenyl ester of N- (2,2-dimethoxyethyl) -4-methylcarbanyl acids 3- (Isopropoxycarbonylamino) -phenyl ef N- (2,2-dimethoxyethyl) -4-methylcarbanilic acid N- (2,2-dimethoxyethyl) -3-methylcarbanilic acid 3- (1-methyl-ethoxycarbonylamino) -phenyl ester Z- (Butoxycarbonylamino) -phenyl ester of N- (2,2-dimethoxyethyl-4-methylcarbanilic acid N- (2,2-dimethoxyethyl) -3-methylcarbanic acid 3- (2-Methylpro-Opoxycarbonylamino) -phenyl ester N- (2,2-dimethoxyethyl) -3-methylcarbanilic acid 3- (1-methylpropoxycarbonylamino) -phenyl ester 3- (2-MethylpropoxycarbonylMino) -phenyl ester of N- (2,2-dimethoxyethyl) -4-methylcarboxylic acid 3- (2-Methoxyethoxycarbonylamino) -phenyl ester of N- (2,2-dimethoxyethyl) -3-methylcarbanic acid Continued tabl, 1 .4 W; . .7179908 Continued table. 1 SG (Allylxycarbonylamino) -phenyl ether - (2,2-dimethoxyethyl) -3-methylcarbanyl Acid. 4 4 3- (2-Propynyloxycarbonylamino) -phenyl ether N- (2,2-dimethoxyethyl) -3-methylcarb-; nil acid. 44 (3-Methylthiocarbonylamino) -phenyl ester of M- (2-methoxyethyl) -carb; yl-yl acid 4 4 3- (Methitibcarbonylamino) -phenyl ester of N- (2,2-dimethoxistil) -4-methyl-capstanil. acid. . . -. . . . (3-Methylthiocarbonylamino) phenyl ether; N- (2,2-Dimethoxyethyl) -3-methylcarbanyl acid, 44- (3-Ethylthiocarbonylamino) -phenyl ester of N- (2,2- | cymethoxyethyl) -3-methylcarbanyl. . acid. -. . , (3-Ethylthiocarbonylamino) -fevyl ester .H- (2,2-dimethoxyxyethyl) -4-methylcarbanyl. ACIDS, -., ... .V - .... .- ... (3-Methylthiocarbonylamino) -phenyl ester of N- (2-ethoxyethyl) -3-methylcarbanyl / i acid, l. V V :::.; -:;, - ;;,; .,. . ; . . - I (3-Methylthiocarbonylamino) -phenyl ether ... N- (2-methoxyethyl) -4-methylcarbamate acid. Mr..:.-....-,. ;.: ...--.;.: -. . (3-Methylthiocarbonylamino) phenyl ester of L (2-butoxyethyl) 4-methylcarbanilic acid. ...: ...,. :. . . . . (3-Methylthiocarbonlamino) -phenyl ester of y- (2-ethoxyethyl) 1-2-MeGlcarbanil-l4 acid:. (3-Methylthiocarbonylamino) -phenyl Ether. (2-methoxyethyl) -3-methoxycarbanilnry4. V. Acids: ..V. . . ; ....... - N- (2-butoxyethyl) -carbanilic acid (5-methylthiocarbonylamino) -phenyl ester "(3-Ethylthiocarbonylakino) -phenyl ester of Y- (2-methoxyethyl) -4-methoxycarbanilic, acid . H- (2-methoxyethyl) -4-methoxycarbanilic acid 3- (1-Methyloxycarbonylamino) phenyl V ester (3-Methylthiocarbonylamino) phenyl ester of K (2-ethoxy-methyl) carbanilic acid 3- (2-ProPhenyloxycarbonylamino-ayloxy-yl-yl-yl-yl-yl-yl-yloxy) -amoylcarboxylic acid; (2-methoxyethyl) -4-methoxycarbacyl-44 hydrochloric acid ,. 3- (1-methylpropoxycarbonylamino) -phenyl, n- (2-methoxyethyl) -4-methoxy of rbanilyic acid ester 3- (2-Methylpropoxycarbonylamino) phenyl ester of N- (2-methoxyethyl) -4-methoxycarbanilic acid N- (2-methoxyethyl) -3-methylcarbanilic acid (3-ethylthiocarbonylamino) phenyl ester. N- (2-methoxyethyl) -3-methylcarbanilic acid 3- (2-methylpropoxycarbonylamino) -phenyl ester 3- (2 / -methylpropoxycarbonylamino) -phenyl ester of N- {2-ethoxyethyl) -carbanilic acid 3- (2-Methylpropoxycarbonylamino) phenyl ester of H- (2-ethoxyethyl) -3-methylcarbanyl 6th acid 3- (1-Methyl Propoxycarbonylamino) Phenyl ester of N- (2-ethoxyethyl) -carbanyl acid N- (2-methoxyethyl) -carbanyl acid 3- (1-cetyl-2-chloroethoxy-carbonylamino) -phenyl ester. 3- (1-Methyl-2-chloro-hydroxycarbonylamino) -phenyl ester of N- (2,2-dimethoxyethyl) -carbanilic acid 3- (Methylthiocarbonylamino) -phenyl ester N- (2-methoxyethyl) -4-meto, xicarbani; 1 Nt: N- (2,2-dimethoxyethyl) -carbanyl acid 3- (2-bromoethoxycarbonylamino) -phenyl ester 3- (2-Methoxyethoxyxy (rboylamino) -phenyl ester of N- (2,2-dimethoxyethide) -carbonyl acid 3- (Methylthiocarbonylamino) -phenyl ester of N- (2-methoxyethyl) -2-methylcarbanyl acids - -..-. l, A „, ..,.-.-. ,, ,, ,, .... H- (2-Propoxyethyl) -3-methylcarbanyl- 3- (2-Methyl Propoxycarbonylamino) -phenyl ester, Noah acid. N- (2-methoxyethyl) -4-methylcarbanilic acid 3- (2-methylpropoxycarbrylamino) -phenyl ester N- (2-methoxyethyl) -3-methyl-carboxylic acid 3- (1-methylpropoxycarbonylamino) phenyl ester. (3-Methylthiocarbonylamino) -phenyl ester of 3-methyl N- (2-propoxyethyl) -carbanilic acid / (3-Allyloxycarbonylamio) -phenyl ester of c- (2-ethoxyethyl) -carbanyl acid Continued table. I 4 4 -., -. - s four four four 1171799012 N- {2-ethoxyethyl) -3-methylcarbanyl (3-allyloxycarbonylamino) -phenyl ester ky eloty. N- (2-Propoxyethyl) -carbanilic acid (3-allyloxycarbonylamino) -phenyl ester 3- (2-Bromoethoxycarbonylamino) -phenyl, ester of H- (methoxyethyl) -carbanilic acid 3- (Methoxycarbonylamino) -phenyl Ely N- (2-butoxyethyl) -3-methylcarbanilic ester 3- (Ethoxycarbonylamino) -phenyl ester of N- (2-but6xyethyl) -3-methylcarbanilic acid 3- (Etoxycarbonylamino) -phenyl ester of N- (2,2-diethoxyethyl) -carbanilic acid 3- (1-Methylethoxycarbonylamino) -phenyl ester of N- (2-prop6xyethyl) -carbanilic acid - 3- (1-Methylethoxycarbonylamino) -phenyl ester of N- (2-butoxyethyl) -3-methylcarbanilic acid N- (2-Propoxyethyl) -3-methylcarbanilic acid 3- (1-Methyltoxycarbonylamino) phenyl ester, 3- (1-Methylethoxycarbonylamino) -phenyl ester of N- (2-butoxyethyl) -4-methylcarbanyl acid 3- (1-Methylethoxycarbonylamino) -phenyl ester of N- (2-butoxyethyl) -carbanyl acid N- (2,2-Diethoxyethyl) -carbanyl acid (3-allyloxycarbonylamino) -phenyl ester 3- (2-Propenyloxycarbonylamino) -phenyl ester of N- (2-methoxyethyl) -2-methylcarbanyl acid 3- (2-Methylpropoxycarbonylamino) phenyl ester of N- (2,2-daethoxyethyl) -carbanilic acid, N- (2,2-diethoxyethyl) -carbanyl 3- (2-Propynyloxycarbonylamino) -phenyl ester acid. ; Z- (Methylthiocarbonylamino) -phenyl ester of N- (2-ethoxyethyl) -4-methylcarbanilic acid 3- (Methylthiocarbonylamino) -phenyl ester of N- (2,2-diethoxyethyl) -carbanilic acid {s-Methylthiocarbonylamino-phenyl ester of N- (2-propoxyethyl) -4-methylcarbanyl acids Continued table. one (3-Methylthiocarbonylamino) phenyl ester of - (2-propoxyethyl) -2-methylcarbanilic acid (3-Methylthiocarbonylamino) phenyl ester of - (2-butoxyethyl) -3-methylcarbanilic acid (3-EthylthiocarbonylsMine6) -phenyl ether. N- (2-propoxyethyl) -3 methylcarbanilic acid. . i. (3-ethylthiocarbonylamino) -phenyl ether - (2-butoxyethyl) -3-methylcarbanilic acid (3-Ethylthiocarbonylamino) -phenyl ether - (2-butoxyethyl) -4-methylcarbanyl acids N- (2-cyanoethyl) -3-chlorocarbayl acid ((Z-allyloxycarbonylamino) -phenyl ester 3- (2-Propyloxycarbonylamino) -phenyl ester of N- (2-propyloxyethyl) -3-methylcarbanilic acid 3- (2-Propynyloxycarbonylamino) -phenyl ester of N- (2-propoxy ethyl) -carbanilic acid 3- (2-Propynyloxycarbonylamine) phenyl ester of H- (2-butoxyet.til) -4-methylcarbanilic acid. N- (2-butoxyethyl) -carbanyl acid 3- (2-PropinyloxycarbonylIlamino) -phenyl ester 3- (2-propynyloxycarbonylamino) -phenyl ester of H- (2-propoxy-yl) -2-methylcarbanilic acid N- (2-Butoxyethyl) -3-methylcarbanilic acid 3- (2-propynyloxycarbonylamino) phenyl ester; N- (2-Propoxyethyl) -4-methylcarbanilic acid 3- (2-propynyloxycarbonylamino) phenyl ester. (3-Ethylthiocarbonylamino) -phenyl ester of - (2-ethoxyethyl) -carbanyl acid (.3-Ethylthiocarbonylamino) -phenyl ester of - (2-ethoxyethyl) -3-methylcarbanilic acid (3-Ethylthiocarbonylamino) -phenyl; o-ester of - (2-propoxyethyl) -2-methylcarbanyl acid (3-Ethylthiocarbonylamino) phenyl ester of N (2-ethoxyethyl) -4-methylcarbanilic acid Continued table. one
权利要求:
Claims (2) [1] V - ipf r #., ": 7 gpk p oprnki- o - no action G4 humiliation SacTe ml ep [2] 2. Experimental plants. PREMIRE 2. Experimental plants 6br2b2yyyyytyy ypiy after exits,. ..., .. ,, -.--: -.----. ,,,., .- .. yormGraskhoDa 1 kg of aytyvnogo-. Begin / ha For comparison, take | 3-mv xycadH nile-3-phenyl 1571799016 ---- G- 1- 1 3 4 -: ..--, -. -J .., -.-: -:., ..-- -.;. , v., -. ,;, -.... -T -.,.; .-. I..i .- .. ji, r ..-. - ,,. .-- L-. ---. - .--.-- ... (3-Ethylthiocarbonylamino) -phenyl ester of M- (2-propoxyethyl) -4-methylcarbanilic acid -: - (3-Ethylthiocarbonylamino) -phenyl ester of N- (2-meToxyethyl) -4 -methylcarb; nyl acid V, (3-Ethylthiocarbonylamino) -phenyl ester of N- (2-ethoxyethyl) -2-methylcarbanilic acid 1. (3-Ethylthiocarbonylamino) -phenyl ester of 1Н- (2-methoxyethyl) -3-methoxycarbanyl acid, -. - (3-Methylthio arbonylamino) -phenyl ester of N- (2-methoxyethyl) -3-methylcarbanilic acid. "...., -, -SZ" L "J (3-Ethoxycarbonylamino) -phenyl ester of 2-methyl L- (2-Propoxyethyl) -carbanilic acid 3- (1-Methylethoxycarbonylamino) phenyl ester of H- (2-ethoxyethyl) carbanyl acid 3- (1-Methyl ethoxycarbonylamino) phenyl ester of H- (2-methoxyethyl) t-4-methyloxyphenyl ester of 3- (2-methoxyethyl) t-4-methyle-phenyl ester of O- (2-methoxyethyl) t-4-methyle) -phenyl ester of O- (2-methoxyethyl) t-4-methyle) -phenyl ester of N- (2-methoxyethyl) t-4-methyyl-phenyl ester of (- (2-methoxyethyl) t-4-methyyl-phenyl ester of - (2-methoxyethyl) t-4-methyyl-phenyl ester of Ы- (2-methoxyethyl) t-4-methyl; acids: N- {2-1-1 -Cisistil) -4-methylcarbanilic acid 3- (1-methyl-ethoxycarbonylamino) -phenyl ester -f3- (1-methyl-ethoxycarbynylamino) -phenyl-1-methyl-1-methyl-1-methyl 1-methyl-1-ester th acid - L. -1--, x- - 3- (1-Methyloethoxycarbonyl-amino-phenyloyl 4-methyl N- (2-prrpoysi9Tyl) ester) -carbanyl acid V i 3 (Ethoxy-arbonylamino) -phenyl 4-methyl-L- ester (2-propO | C IETHYL) -carbanilic acid. 3- (1-Methyl ethoxycarbonylgarynol) -phenyl ester IN- (2-ethoxyethyl-3-methyLcarbanillic acid; 3- {1-Methyl ethoxycarbonylamino) -phenyl ester S- ( 2-ethoxyethyl) -2-methylcarbanilic acid Continued table. 1 3-methylcarbanilic ester (Compound A). The plants were 60 In the early stage of development. Liquids take 500 l / ha. Means nands t .., .. g - "-.-, l" in the form of a water emulsion, after 14 days - .. .. .. 1. "" Tk. I l evaluate the results of processing. Rating scale: 10 - no damage; About - the destruction of plants. 17 In table. 2 shows comparative data on the herbicidal activity of the proposed and known compounds. It has been shown that when compatible with cultivated plants of the ped. Table 2 of these compounds achieve a good effect on the weeds, while the comparative remedy severely damages cultivated plants. 19 Claims Herbicidal agent containing a derivative of carbamic acid as an active principle, as well as auxiliary components, selected from a group of liquid or solid carriers of surfactants, with the aim of increasing herbicidal activity and improve the selectivity of action, as a carbamic acid derivative, a compound of the general formula € # 4 B5 - 0 de R - alkyl C; - Qj, 2-methoxyethyl, hlrethyle, bromoethyl, chloro; Isopropyl, ally, propargyl; R - alkoxyethyl, 2,2-dimethoxyethyl, 2,2-diethoxyethium; R is MeTHJi or Metxy; p - O or I) to acid 6) rb or, in an amount from GO to 80 wt.%. Sources of information taken into account in the examination 1.Patent of the Federal Republic of Germany 1567151 cl. 12 about 17/01, publ. 21.b2.74, 2.Patent of Germany W2310648, kL. 12 from 17/01, 19.09.74 (prototype).
类似技术:
公开号 | 公开日 | 专利标题 SU717990A3|1980-02-25|Herbicidic agent SU655278A3|1979-03-30|Insecticide DE2163391C3|1980-08-28|Pesticidal phosphorothiolate compounds US4072751A|1978-02-07|Pesticidal N-substituted bis-carbamoyl sulfide compounds US4096269A|1978-06-20|N-haloalkane-sulfenylcarbamoyl oxime pesticides US3470299A|1969-09-30|2-methyl-coumaran-7yl-n-methyl-carbamate DE2617736C2|1982-12-09|Pesticides US4138423A|1979-02-06|N-dithio carbamoyl oximes US7511029B2|2009-03-31|Pesticidal diazene oxide carboxylates DE1567142C3|1975-07-24|Oxime carbamates and their use as insecticides, akaricides and nematicides Davies et al.1948|Chemical constitution and insecticidal action. 1. Organic sulphur compounds CA1091686A|1980-12-16|Thiophosphorylguanidines for combating pests US3476490A|1969-11-04|Methods of using particular carbamic acid esters for insecticidal and acaricidal purposes US3450818A|1969-06-17|Simultaneously effective antifungal and insecticidal or acaricidal pesticides US2811476A|1957-10-29|Phosphorus derivatives, process for their preparation, and compositions containing them US3726973A|1973-04-10|1-alkoxy|-1-thiono-3-chloro| phospholines compositions and their use US4188400A|1980-02-12|Furylmethyloxime ethers SU607529A3|1978-05-15|Herbicide US4219547A|1980-08-26|Phosphoroimidophenyl insecticides US4062951A|1977-12-13|Organophosphorus compounds, compositions containing them and their method of use DE2232076A1|1973-01-18|ORGANIC PHOSPHORIC ACID ESTERS, PROCESS FOR THEIR PRODUCTION AND THEIR USE AS INSECTICIDES, ACARICIDES AND NEMATOCIDES SU668564A3|1979-06-15|Herbicide US3406179A|1968-10-15|1-|-2-imidazolidone s-| US3083135A|1963-03-26|Phosphorus-containing thioureas US3081340A|1963-03-12|Dihydronaphthyl n-methyl-carbamates
同族专利:
公开号 | 公开日 IT7825741D0|1978-07-17| CA1103268A|1981-06-16| AU519399B2|1981-12-03| PL111138B1|1980-08-30| IT1097530B|1985-08-31| CS197327B2|1980-04-30| FR2398053B1|1982-11-19| BE869074A|1979-01-18| GB2002356B|1982-03-03| JPS5422340A|1979-02-20| FR2398053A1|1979-02-16| DD137822A5|1979-09-26| CH637372A5|1983-07-29| GR73026B|1984-01-25| IL55156A|1982-11-30| IE47234B1|1984-01-25| DK320778A|1979-01-19| PL208435A1|1979-03-26| GB2002356A|1979-02-21| PT68309A|1978-08-01| ES471736A1|1979-02-01| US4441915A|1984-04-10| NL7807482A|1979-01-22| IE781440L|1979-01-18| HU180531B|1983-03-28| SU858561A3|1981-08-23| LU79980A1|1978-12-12| AU3810478A|1980-01-24| IL55156D0|1978-09-29| DE2732848A1|1979-02-08|
引用文献:
公开号 | 申请日 | 公开日 | 申请人 | 专利标题 US3133808A|1959-03-16|1964-05-19|Monsanto Chemicals|Herbicide composition| US3404975A|1964-12-18|1968-10-08|Fmc Corp|m--carbanilates as herbicides| DE1567151C3|1965-04-09|1974-02-21|Schering Ag, 1000 Berlin Und 4619 Bergkamen|Diurethanes, processes for the preparation of these compounds and herbicidal compositions containing them| US3551477A|1966-07-06|1970-12-29|Basf Ag|Novel biscarbamates| US3901936A|1966-10-15|1975-08-26|Schering Ag|Process for the preparation of n-carbamoyloxyphenyl carbamates| US3865867A|1967-06-19|1975-02-11|Monsanto Co|Meta-bifunctional benzenes| DE2108975C3|1971-02-16|1979-12-20|Schering Ag, 1000 Berlin Und 4619 Bergkamen|N-acyl diurethanes and herbicidal agents containing them| EG10699A|1971-06-23|1976-07-31|Bayer Ag|Novel n.carbamic aryl acid esters method for preparation and their use for controlling plant growth| US4022611A|1972-06-06|1977-05-10|Ciba-Geigy Corporation|Plant growth regulating agent| US3997325A|1973-05-24|1976-12-14|American Cyanamid Company|alkyl and alkyl carbamates and their use as herbicides| US3976470A|1975-07-23|1976-08-24|Stauffer Chemical Company|Diphenyl ether amides|IE50640B1|1980-04-28|1986-05-28|Stauffer Chemical Co|Synergistic herbicidal compositions and use thereof| GR78909B|1982-08-13|1984-10-02|Sipcam Spa| US6150328A|1986-07-01|2000-11-21|Genetics Institute, Inc.|BMP products| JP3504263B2|1991-11-04|2004-03-08|ジェネティックス・インスチチュート・リミテッド・ライアビリティ・カンパニー|Recombinant bone morphogenetic protein heterodimers, compositions and uses| US20080070842A1|1991-11-04|2008-03-20|David Israel|Recombinant bone morphogenetic protein heterodimers, compositions and methods of use| US6291206B1|1993-09-17|2001-09-18|Genetics Institute, Inc.|BMP receptor proteins| PT733109E|1993-12-07|2006-07-31|Genetics Inst Llc|MORPHOGENETIC PROTEINS OF 0SS0S PMO-12 AND PMO-13 AND THEIR COMPOSITIONS FOR TENDAO INDUCTION| US6727224B1|1999-02-01|2004-04-27|Genetics Institute, Llc.|Methods and compositions for healing and repair of articular cartilage| DK1223990T3|1999-10-15|2004-11-29|Inst Genetics Llc|Formulations of hyaluronic acid for delivery of osteogenic proteins| US20030082233A1|2000-12-01|2003-05-01|Lyons Karen M.|Method and composition for modulating bone growth| US7226587B2|2001-06-01|2007-06-05|Wyeth|Compositions and methods for systemic administration of sequences encoding bone morphogenetic proteins| TWI267378B|2001-06-08|2006-12-01|Wyeth Corp|Calcium phosphate delivery vehicles for osteoinductive proteins| BR0310087A|2002-05-17|2005-08-16|Wyeth Corp|Hyaluronic acid injectable solid carriers for application of osteogenic proteins| AU2004272072B2|2003-09-12|2010-07-08|Etex Corporation|Injectable calcium phosphate solid rods and pastes for delivery of osteogenic proteins|
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申请号 | 申请日 | 专利标题 DE19772732848|DE2732848A1|1977-07-18|1977-07-18|DIURETHANE, HERBICIDAL AGENTS CONTAINING THESE COMPOUNDS AND THE PROCESS FOR THEIR PRODUCTION| 相关专利
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