Abstract: Compounds formed by combining a carboxylic acid herbicide with N—((C1-C16) alkyl or arylalkyl) tri((C1-C16) alkyl)ammonium hydroxide have herbicidal activity on an acid equivalent basis at least as active as the commercially used carboxylic acid herbicide salts, but are less volatile.

Abstract: Compounds formed by combining a carboxylic acid herbicide with N-((C1-C16) alkyl or arylalkyl) tri((C1-C16) alkyl)ammonium hydroxide have herbicidal activity on an acid equivalent basis at least as active as the commercially used carboxylic acid herbicide salts, but are less volatile.

Abstract: Compounds formed by combining a carboxylic acid herbicide with N—((C1-C16) alkyl or arylalkyl) tri((C1-C16) alkyl)ammonium hydroxide have herbicidal activity on an acid equivalent basis at least as active as the commercially used carboxylic acid herbicide salts, but are less volatile.

Abstract: Compounds formed by combining a carboxylic acid herbicide with N-((C1-C16)alkyl or arylalkyl) tri(C1-C16)alkyl)ammonium hydroxide have herbicidal activity on an acid equivalent basis at least as active as the commercially used carboxylic acid herbicide salts, but are less volatile.

Abstract: Compounds formed by combining a carboxylic acid herbicide with N—((C1-C16)alkyl or arylalkyl) tri((C1-C16)alkyl)ammonium hydroxide have herbicidal activity on an acid equivalent basis at least as active as the commercially used carboxylic acid herbicide salts, but are less volatile.

Abstract: Compounds formed by combining a carboxylic acid herbicide with N—((C1-C16) alkyl or arylalkyl) tri((C1-C16) alkyl)ammonium hydroxide have herbicidal activity on an acid equivalent basis at least as active as the commercially used carboxylic acid herbicide salts, but are less volatile.

Abstract: The present invention relates to fungicidal compositions and their use for controlling oomycete pathogen induced disease or diseases in one or more plants.

Abstract: Disclosed herein are acylhydrazone and semicarbazones derivatives of aldehydes and ketones that may act to attract plant pathogenic zoospores and methods of using these compounds. These compounds include the compound according to Formula 1: wherein: X is selected from the group consisting of: (CH2)n, 1,3-phenylene and 1,4-phenylene; R1 is selected from the group consisting of iso-butyl, sec-butyl and tert-butyl-CH2; R2 is hydrogen or methyl; and n is equal to 0-25. Upon exposure to water, these compounds release aldehydes or ketones that may attract zoospores. These compounds can be combined with fungicides to form fungicidal formulations that are especially effective against oomycete producing fungal pathogens.

Abstract: The present invention relates to compounds and the use of such compounds for increasing the efficacy of fungicides for controlling oomycete pathogen induced disease or diseases in one or more plants.

Abstract: Compounds formed by combining a carboxylic acid herbicide with N—((C1-C16)alkyl or arylalkyl) tri((C1-C16)alkyl)ammonium hydroxide have herbicidal activity on an acid equivalent basis at least as active as the commercially used carboxylic acid herbicide salts, but are less volatile.

Abstract: Ionic liquids, formed by combining a carboxylic acid herbicide with certain trialkylamines or heteroarylamines, have herbicidal activity on an acid equivalent basis at least as active as the commercially used carboxylic acid herbicide salts, but are less volatile.

Abstract: A composition comprising at least one bisdithiocarbamate fungicide and at least one zinc additive is provided. Processes related thereto are also provided.

Abstract: A composition comprising at least one bisdithiocarbamate fungicide and at least one zinc additive is provided. Processes related thereto are also provided.

Abstract: New synthetic procedures for preparing insecticidal 3-(substituted phenyl)-5-(thienyl or furyl)-1,2,4-triazoles utilizing thioimidate intermediate.

Abstract: 3-(Substituted phenyl)-5-(thienyl)-1,2,4-triazole compounds are useful as insecticides and acaricides.

Abstract: Alkyl 3-chloroanthranilates are the major product from the chlorination of alkyl esters of anthranilic acid with 1,3-dichloro-5,5-dimethylhydantoin. The 3-chloro isomer can be readily separated from the accompanying 5-chloro isomer by selective acetylation of the latter.

Abstract: N-(Substituted-phenyl)-7-ethoxy-5-fluoromethyl-1,2,4-triazolo[1,5-a]pyrimid ine-2-sulfonamides are prepared from 2-benzylthio-5-fluoromethyl-1,2,4-triazolo[1,5-a]pyrimidines and found to be herbicidal. The compounds, illustrated by 7-ethoxy-5-fluoromethyl-(2,6-dichloro-3-methylphenyl)-1,2,4-triazolo[1,5-a ]-pyrimidine-2-sulfonamide, are degradable in the soil and are selective to wheat.

Abstract: A method for preparing substituted phenoxyphenols which are useful in the preparation of herbicidal (phenoxyphenoxy)propionates is disclosed. The process involves the oxidation of substituted phenoxyphenones to the corresponding phenoxyphenyl esters and their conversion to the desired phenoxyphenol. Novel intermediates for the process are similarly disclosed.

Abstract: Novel substituted triazolo [1,5-a]pyrimidine-2-sulfonamides, e.g., 5,7-dimethyl-N-(2,6-dichlorophenyl)-1,2,4-triazolo[1,5-a]pyrimidine-2-sulf onamide and their agriculturally acceptable salts are prepared. These compounds and compositions containing them are useful for the control of unwanted vegetation. Novel substituted triazolo[1,5-a]pyrimidine-2-sulfonyl chlorides and substituted anilines and their use as intermediates are also described.

Abstract: N-(Substituted-phenyl)-5-fluoromethyl-1,2,4-triazolo[1,5-a]pyrimidine-2-sul fonamides are prepared from 2-benzylthio-5-fluoromethyl-1,2,4-triazolo[1,5-a]-pyrimidines and found to be herbicidal. The compounds, illustrated by 5-fluoromethyl-7-methoxy-(2,6-dichloro-3-methylphenyl)-1,2,4-triazolo[1,5- a]pyrimidine-2-sulfonamide, are degradable in the soil.