62235-99-8

Usage

Structure

Aromatic amine with a pyrazole ring substituted with a phenyl group at the 1-position and three methyl groups at the N and N3 positions.

Usage

Commonly used in organic synthesis and pharmaceutical research as a building block for the synthesis of various biologically active compounds.

Pharmacological properties

Known for its potential pharmacological properties and has been studied for its potential use in the development of new drugs.

Applications

In addition to pharmaceuticals, it has applications in the field of agrochemicals and materials science.

Upstream product

• 124-40-3 dimethyl amine 
• 5499-69-4 5-dimethylamino-3-methyl-1-phenyl-1H-pyrazole-4-carbaldehyde 
• 20568-22-3 4-(dimethylamino)but-3-yn-2-one 
• 100-63-0 phenylhydrazine 

Relevant academic research and scientific papers

Facile microwave assisted decarbonylation of 4-formyl group in 5-alkyl amino substituted pyrazoles

Facile decarbonylation of the 4-formyl group in 5-alkyl amino pyrazoles was seen when reacted with catalytic p-toluene sulfonic acid in methanol under microwave irradiation to provide parent 4-H pyrazoles in good yields.

REACTION OF 1-DIALKYLAMINO-1-BUTYN-3-ONES WITH HYDRAZINE AND SUBSTITUTED HYDRAZINES

A series of 1-dialkylmino-1-butyn-3-ones were obtained, and their reactions with hydrazine and its alkyl, aryl and unsymmetrical dialkyl derivatives were studied.The reactions with unsubstituted and monosubstituted hydrazones lead to the formation of heterocyclic compounds of the pyrazole series, while the monosubstituted hydrazines form two isomeric products.Unsymmetrical dimethylhydrazine adds at the C1-carbon atom with the formation of compounds containing an open structure.