21452-18-6

Usage

Uses

Used in Agricultural Industry:
2,4-Dimethyl-N-phenyl-5-thiazolecarboxamide is utilized as a fungicide and pesticide for its capability to inhibit the growth of fungi and certain pests. It operates by disrupting the metabolic processes of the target organisms, which results in their death. Due to its moderate toxicity, it is essential to exercise caution during its application to ensure safety and effectiveness.

InChI:InChI=1/C12H12N2OS/c1-8-11(16-9(2)13-8)12(15)14-10-6-4-3-5-7-10/h3-7H,1-2H3,(H,14,15)

Upstream product

• 53137-27-2 2,4-dimethyl-thiazole-5-carboxylic acid 
• 62-53-3 aniline 

Downstream Products

• 931400-07-6 N-[(2,4-dimethyl-1,3-thiazol-5-yl)methyl]aniline 
• 118-69-4 2,6-dichlorotoluene 
• 3260-88-6 1-chloro-3-methoxy-2-methylbenzene 

Relevant academic research and scientific papers

PROLYL HYDROXYLASE ANTAGONISTS

This invention relates to certain 2-[(quinolin-3-yl)carbonyl]aminoacetic acid derivatives of formula (I), where the various groups are defined herein, and which are useful in treating anemia.

Arylphenyl-substituted cyclic keto enols

The present invention relates to novel arylphenyl-substituted cyclic ketoenols, their preparation and the use of such ketoenols as pesticides and/or herbicides. The novel arylphenyl-substituted cyclic ketoenols are of the formula (I) in which CKE refers to the cyclic ketoenol and W, X, Y and Z are as defined in the specification.

Process for synthesizing benzoic acids

A nucleophilic substitution reaction on optionally substituted dihalobenzenes is carried out in the presence of an optional catalyst followed by formation of and subsequent carboxylation of a Grignard reaction intermediate. In particular the present invention provides a process leading to optionally substituted hydroxybenzoic, alkanoyloxybenzoic, formyloxybenzoic and alkoxybenzoic acids from 1-substituted 2,6-dihalobenzenes. The invention also provides a process for the direct formation of an acyl chloride from a Grignard reagent by quenching with phosgene.

Process for synthesizing benzoic acids

Nucleophilic substitution reactions on halobenzenes or triflyl substituted benzenes are carried out in the presence of catalysts. In particular the present invention provides a process leading to optionally substituted hydroxybenzoic, alkanoyloxybenzoic, formyloxybenzoic and alkoxybenzoic acids and optionally substituted hydroxybenzonitriles and alkoxybenzonitriles from substituted 2,6-dihalobenzenes, 2-halo-6-triflylbenzene and 2,6-ditriflylbenzenes.

Process for synthesizing benzoic acids

Nucleophilic substitution reactions on halobenzenes are carried out in the presence of catalysts. In particular the present invention provides a process leading to optionally substituted hydroxybenzoic and alkoxybenzoic acids and optionally substituted hydroxybenzonitriles and alkoxybenzonitriles from substituted 2,6-dihalobenzenes.