221564-97-2

Usage

General Description

2,2-dichloro-12-(4-chlorophenyl)dodecanoic acid is a synthetic compound that consists of a dodecanoic acid backbone with two chlorine atoms attached to the 2nd carbon and a 4-chlorophenyl group attached to the 12th carbon. It is mainly used as a pesticide and herbicide in agricultural applications due to its ability to disrupt the growth and development of various plant species. The compound works by interfering with the production of fatty acids in the targeted plants, leading to their eventual death. 2,2-dichloro-12-(4-chlorophenyl)dodecanoic acid is classified as a chlorinated aliphatic acid and should be handled with caution due to its toxic and potentially harmful effects on the environment and human health.

Upstream product

• 79-43-6 dichloro-acetic acid 
• 178671-35-7 1-Bromo-10-(4-chlorophenyl)-decane 
• 4101-68-2 1,10-dibromodecane 
• 800395-33-9 methyl 2,2-dichloro-12-(4-chlorophenyl)-dodecanoate 
• 914481-25-7 t-butyl 2,2-dichloro-12-(4-chlorophenyl)dodecanoate 
• 873-77-8 (4-chlorphenyl)magnesium bromide 

Downstream Products

• 800395-33-9 methyl 2,2-dichloro-12-(4-chlorophenyl)-dodecanoate 

Relevant academic research and scientific papers

METHOD FOR PRODUCING 2,2-DICHLORO-12-(4-HALOPHENYL)DODECANATE SALT AND METHOD FOR PRODUCING PRODUCTION INTERMEDIATE THEREOF

Disclosed is a commercially suitable method for producing a 1-substituted-10-(4-halophenyl)decane with high yield in a short time without producing 4,4'-dichlorobiphenyl (an environmental pollutant). Also disclosed is a commercially suitable method for producing a 2,2-dichloro-12-(4-halophenyl)dodecanate salt with high yield by a simple process. Specifically disclosed is a method for producing a 1-substituted-10-(4-halophenyl)decane characterized by reacting a 4-halobenzylmagnesium halide with a 1,9-disubstituted nonane. Also specifically disclosed is a method for producing a 2,2-dichloro-12-(4-halophenyl)dodecanate salt characterized by comprising a first step for obtaining a 2,2-dichloro-12-(4-halophenyl)dodecanoic acid ester by reacting a 1-iodo-10-(4-halophenyl)decane and a dichloroacetic acid ester in the presence of a base, and a second step for converting the 2,2-dichloro-12-(4-halophenyl)dodecanoic acid ester into a 2,2-dichloro-12-(4-halophenyl)dodecanate salt. Further specifically disclosed are 1-iodo-10-(4-chlorophenyl)decane and a method for producing the same.

2,2-Dichloroalkanecarboxylic acids, processes for their production and pharmaceutical agents containing these

Pharmaceutical agents for treating diabetus mellitus which contain a compound of formula I STR1 as the active substance, in which A, B, A' and W have the meanings stated in the claims, new compounds of formula I as well as processes for their production.

ω-Substituted alkyl carboxylic acids as antidiabetic and lipid-lowering agents

In screening experiments certain ω-substituted alkyl carboxylic acids were found to produce an increase in insulin-stimulated 14C-acetate incorporation into triglycerides, which may indicate an improvement in the action of insulin. Antidiabetic