35887-72-0

Usage

Uses

Used in Pharmaceutical Industry:
4-chloro-2,6-dimethylbenzoic acid is used as an intermediate in the synthesis of pharmaceutical compounds for its ability to be incorporated into the molecular structures of various drugs. Its unique properties allow for the development of new medications with specific therapeutic effects.
Used in Agrochemical Industry:
In the agrochemical sector, 4-chloro-2,6-dimethylbenzoic acid is utilized as a building block for the creation of agrochemicals, such as pesticides and herbicides. Its chemical structure contributes to the effectiveness of these products in controlling pests and unwanted plant growth.
Used in Organic Synthesis:
4-chloro-2,6-dimethylbenzoic acid serves as a valuable intermediate in organic synthesis processes due to its reactive functional groups and unique structural features. It can be used to synthesize a wide range of chemical compounds for various applications, including specialty chemicals and materials.

Upstream product

• 35887-71-9 1-(4-chloro-2,6-dimethylphenyl)ethanone 
• 110-05-4 di-tert-butyl peroxide 
• 7499-07-2 4-chloro-2-methylbenzoic acid 
• 35887-70-8 2-(4-chloro-2,6-dimethyl-phenyl)-6-methyl-pyran-4-one 
• 5757-67-5 4-chloro-2,6-dimethylbenzonitrile 
• 85374-88-5 4-Chlor-2,6-dimethylbenzamid 

Downstream Products

• 632-46-2 2,6-dimethylbenzoic acid 
• 306296-04-8 C₃₅H₄₁ClF₃N₃O₂ 
• 85374-86-3 4-Chlor-2,6-dimethylbenzoesaeure-trifluormethansulfonsaeure-anhydrid 
• 85374-81-8 4-Chlor-2,6-dimethylbenzoesaeure-methansulfonsaeure-anhydrid 
• 85374-64-7 4-Chlor-2,6-dimethylbenzoylchlorid 

Relevant academic research and scientific papers

Preparation method for o-tolylacetic acid aryl formic acid derivative

The invention discloses a preparation method for an o-tolylacetic acid aryl formic acid derivative. According to the method, new C-C bonds can be formed, the organic o-tolylacetic acid aryl formic acid derivative is obtained, the good functional group tolerance is achieved, and the o-tolylacetic acid aryl formic acid derivative which cannot be easily obtained by adopting other methods can be synthesized; according to the method, adopted raw materials are easy to obtain, the yield is high, the reaction conditions are mild, the substrate range is wide, and after-treatment is simple and green.

Palladium-Catalyzed ortho-C-H Methylation of Benzoic Acids

A palladium-catalyzed methylation of C-H bonds of benzoic acids with di-tert-butyl peroxide as the methylating reagent under an external oxidant and ligand-free conditions has been achieved. The reaction is found to be directed by a weakly coordinating carboxyl group, offering a facile route for the synthesis of highly functionalized ortho-methyl benzoic acids.

PIPERAZINE DERIVATIVES USEFUL AS CCR5 ANTAGONISTS

The use is described of CCR5 antagonists of formula (I) or a pharmaceutically acceptable salt thereof, wherein: R is optionally substituted phenyl, pyridyl, thiophenyl or naphthyl; R 1 is hydrogen or alkyl; R 2 is substituted phenyl, substituted heteroary

Piperazine derivatives useful as CCR5 antagonists

The use of CCR5 antagonists of the formula or a pharmaceutically acceptable salt thereof, wherein R is optionally substituted phenyl, pyridyl, thiophenyl or naphthyl; R1is hydrogen or alkyl; R2is substituted phenyl, substituted heter

Carboxylic Trifluoromethanesulfonic and Methanesulfonic Anhydrides, Synthesis and Dissociation Tendency

Carbonyl chlorides 1 react with silver trifluoromethanesulfonate (2) and silver methanesulfonate (6) to give carboxylic trifluoromethanesulfonic anhydrides 3 and carboxylic methanesulfonic anhydrides 7, resp., in good yields; the anhydrides 3 may be synth