331727-49-2

Usage

Uses

Used in Pharmaceutical Applications:
1-(4-Methylphenyl)-5-oxopyrrolidine-3-carbohydrazide is used as a pharmaceutical compound for its potential anti-inflammatory and analgesic effects. It is being studied for its ability to alleviate pain and reduce inflammation, which could make it a valuable addition to the medical field.
Used in Organic Synthesis:
1-(4-Methylphenyl)-5-oxopyrrolidine-3-carbohydrazide is used as a building block in organic synthesis for its unique molecular structure. Its pyrrolidine ring and carboxylic acid group make it a promising candidate for the development of new compounds and materials in the chemical industry.

Upstream product

• 133747-58-7 methyl 5-oxo-1-(p-tolyl)pyrrolidine-3-carboxylate 

Downstream Products

• 956593-23-0 C₁₉H₁₈N₄O₄ 
• 956593-24-1 C₁₉H₁₉N₃O₃ 
• 956593-22-9 C₁₉H₁₈BrN₃O₂ 
• 956593-25-2 C₂₁H₂₄N₄O₂ 
• 956593-17-2 C₁₅H₁₉N₃O₂ 
• 956593-20-7 C₁₇H₁₉N₃O₂ 
• 1342800-40-1 N'-(3-chloro-1,4-dioxo-1,4-dihydronaphthalen-2-yl)-1-(4-methylphenyl)-5-oxopyrrolidine-3-carbohydrazide 
• 1342800-36-5 N-ethyl-N'-(3-methyl-4-oxo-1,4-dihydronaphthalen-1-yl)-1-(4-methylphenyl)-5-oxopyrolidine-3-carbohydrazide 
• 1342800-29-6 N'-(3-methyl-4-oxo-1,4-dihydronaphthalen-1-ylidene)-1-(4-methylphenyl)-5-oxopyrrolidine-3-carbohydrazide 
• 1342800-22-9 1-(4-methylphenyl)-5-oxo-N'-(4-oxo-1,4-dihydronaphthalen-1-ylidene)pyrrolidine-3-carbohydrazide 

Relevant academic research and scientific papers

Reactions of 5-oxo-1-phenylpyrrolidine-3-carbohydrazides with 1,4-naphthoquinone derivatives and the properties of the obtained products

N′-(4-Oxo-1,4-dihydronaphthalen-1-ylidene)-1-phenyl-5-oxopyrrolidine- 3-carbohydrazides and N′-(3-methyl-4-oxo-1,4-dihydronaphthalen-1-ylidene)- 1-phenyl-5-oxopyrrolidine-3-carbohydrazides were synthesized by reactions of 5-oxo-1-phenylpyrrolidine-3-carbo

Synthesis and investigation of some 1,4-disubstituted 2-pyrrolidinones

A series of condensation products of 1-aryl-4-hydrazinecarbonyl-2- pyrrolidinones with acetone, 2,4-pentanedione, and aromatic aldehydes was obtained and identified by the combination of IR, mass and 1H, 13C NMR spectroscopy. The results of their structural studies by NMR spectroscopy are provided. It was ascertained that the presence of the NH group determines the existence of the mixtures of the Z/E-isomers of compounds under study. The availability of Z-isomer as a sterically favorable one was also verified by computer molecular modeling. Springer Science+Business Media, Inc. 2006.