143417-47-4

Basic information

• Product Name: 5(4H)-Oxazolone, 2-methyl-4-(phenylmethylene)-, (4E)-
• Synonyms: 2-methyl-5-benzylidene-5-oxazolone;4-benzylidene-2-methyloxazolidin-5-one;4-benzylidene-2-methyl-5-oxazolone;4-benzylidene-2-methyl-4H-oxazol-5-one;2-methyl-4-benzylidene-1,3-oxazolin-5-one;2-methyl-4-benzylidene-5-oxazolone
• CAS NO: 143417-47-4
• Molecular Formula: C11H9NO2
• Molecular Weight: 187.198
• Mol File: 143417-47-4.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 5(4H)-Oxazolone, 2-methyl-4-(phenylmethylene)-, (4E)-(CAS DataBase Reference)
• NIST Chemistry Reference: 5(4H)-Oxazolone, 2-methyl-4-(phenylmethylene)-, (4E)-(143417-47-4)
• EPA Substance Registry System: 5(4H)-Oxazolone, 2-methyl-4-(phenylmethylene)-, (4E)-(143417-47-4)

Safety Data

• Hazardous Substances Data: 143417-47-4(Hazardous Substances Data)

Upstream product

• 100-52-7 benzaldehyde 
• 38879-46-8 (Z)-4-benzylidene-2-methyl-5(4H)-oxazolone 
• 543-24-8 N-acetylglycine 

Downstream Products

• 38879-46-8 (Z)-4-benzylidene-2-methyl-5(4H)-oxazolone 
• 55636-11-8 (E)-2-Acetylamino-N-benzyl-3-phenyl-acrylamide 
• 136809-72-8 4-benzylidene-1-(4-hydroxy-3-piperidinomethylphenyl)-2-methylimidazolidin-5-one 

Relevant articles and documents

Benzylidene-oxazolones as molecular photoswitches

The synthesis and photochemical study of a family of molecular switches inspired by the green fluorescent protein (GFP) chromophore is presented. These compounds can be easily synthesized, and their photophysical properties may be tuned. Due to their effi

CARBONIC ANHYDRASE INHIBITORS

Compounds are provided which are inhibitors of the CAXII enzyme. Due to the interaction between CAXII and Pgp, such compounds may be useful in lowering the chemoresistance of a cancer allowing for co-administration with existing anti-cancer agents.

Reaction of 4-Benzylidene-2-methyl-5-oxazolone with Amines, Part 2: Influence of substituents in para-position in the phenyl ring and a substituent on Amine Nitrogen Atom on the reaction kinetics

An influence of a structure of the amine (benzylamine, N-methyl-benzylamine, N-isopropyl-benzylamine, N-methyl-butylamine, N-ethyl-butylamine, sec-butylamine, and tert-butylamine) on a rate constant of the ring-opening reaction of 4-benzylidence-2-methyl-