19508-16-8

Usage

Class

Amide

Structure

Contains a diphenylmethyl group

Uses

Organic synthesis and pharmaceutical research
Potential as an anti-inflammatory agent
Potential antitumor properties

Specific content

Member of the amide class of compounds
Structure contains a diphenylmethyl group
Uses in organic synthesis and pharmaceutical research
Potential as an anti-inflammatory agent
Potential antitumor properties
Subject of research in medicinal chemistry

Upstream product

• 49659-69-0 4-benzylidene-2-styryloxazolin-5-one 
• 62-53-3 aniline 
• 1750-36-3 (E)-N-benzylidenebenzenamine 
• 16534-24-0 (E)-cinnamoylglycine 
• 115127-03-2 N-cinnamoylamino glycine 
• 16534-24-0 N-cinnamoylglycine 
• 100-52-7 benzaldehyde 

Relevant academic research and scientific papers

A fast and facile synthesis of n-substituted 2-acylaminoprop-2- enamides using unsaturated azlactones as synthons

A modified route for the fast and facile synthesis of N-substituted 2-acylaminopro- 2-enamides (4) is hereby developed. The conversion of α -N-acylglycine (1) to unstable 2-substituted 2-oxazolin-5-ones (2) was carried out at room temp using ptoluenesulph

Condensation of 4-Benzylidene-2-methyloxazolin-5-one with Schiff Bases: Formation of 1-Aryl-4-benzylidene-2-styrylimidazolin-5-ones

Condensation of 4-benzylidene-2-methyloxazolin-5-one (II) with schiff bases (I) in acetic acid results in 1-aryl-4-benzylidene-2-styrylimidazolin-5-ones (III) and α-acetamidocinnamanilides (IV), characterised by spectral, analytical and chemical methods.