6392-25-2

Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
DCMM is utilized as a precursor in the synthesis of various pharmaceuticals and agrochemicals, contributing to the development of new drugs and pesticides. Its chemical properties allow it to be a key component in creating effective and innovative products in these industries.
Used in Antifungal and Antibacterial Applications:
DCMM has been studied for its potential antifungal and antibacterial properties, making it a candidate for use in treatments and products aimed at combating infections caused by fungi and bacteria.
Used in Material Science:
As a building block, DCMM has been explored for its potential use in the development of new materials, suggesting its applicability in creating novel substances with unique properties for various applications.
Used in Organic Synthesis:
DCMM also serves as a reagent in organic synthesis, facilitating chemical reactions that lead to the formation of desired products. Its versatility in this context highlights its importance in the advancement of organic chemistry.

Upstream product

• 110-91-8 morpholine 
• 89-75-8 2,4-dichlorobenzoyl chloride 
• 50-84-0 2,4 dichlorobenzoic acid 

Downstream Products

• 154046-98-7 (2,4-dichlorophenyl)(1H-pyrrol-2-yl)methanone 
• 154047-17-3 (2,4-Dichloro-phenyl)-(1H-pyrrol-2-yl)-methanol 
• 154047-04-8 (1-Allyl-1H-pyrrol-2-yl)-(2,4-dichloro-phenyl)-methanone 
• 154047-23-1 (1-Allyl-1H-pyrrol-2-yl)-(2,4-dichloro-phenyl)-methanol 

Relevant academic research and scientific papers

Design, synthesis and evaluate in vitroantifungal activity of novel benzamide derivatives

Summary: A series of novel benzamide derivatives according to fluopicolide were designed and synthesized following the rule of combination carboxylic acid amides and amines derivatives together. The antifungal activity of the 15 new compounds were evaluated in vitroagainst five pathogenic fungi, including Sclerotinia sclerotiorum,Gibberella zeae, Rhizoctonia solani, Helminthosporium maydisand Botrytis cinerea. Almost all the structure have not been reported, except compounds 3, 5and 6. A surprising finding is that all the five tested fungi breed faster than negative controls when supplementary with compound 7-15, respectively.

Process for preparing 5-aroyl-1,2-dihydro-3H-pyrrolo[1,2-A]pyrrole-1,1-dicarboxylates

5-Aroyl-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1,1-dicarboxylates of the formula STR1 are prepared from 2-halopyrroles. Hydrolysis and β-decarboxylation of these compounds affords ketorolac and related compounds.

Process for 5-aroylation of 1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-carboxylic esters

An improved process for 5-aroylation of 1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-carboxylic esters and nitriles and for subsequent hydrolysis thereof is disclosed. In the improved process, an aroyl morpholide is reacted with the pyrrolo pyrrole system and the resultant decomposed with base.