291313-34-3

Basic information

• Product Name: methyl 3-(4-hydroxyphenyl)propionate-benzylimide
• Synonyms: methyl 3-(4-hydroxyphenyl)propionate-benzylimide
• CAS NO: 291313-34-3
• Molecular Weight: 269.343
• Mol File: 291313-34-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: methyl 3-(4-hydroxyphenyl)propionate-benzylimide(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 3-(4-hydroxyphenyl)propionate-benzylimide(291313-34-3)
• EPA Substance Registry System: methyl 3-(4-hydroxyphenyl)propionate-benzylimide(291313-34-3)

Safety Data

• Hazardous Substances Data: 291313-34-3(Hazardous Substances Data)

Upstream product

• 291313-49-0 N-benzyl-3-(4-acetoxyphenyl)propionamide 
• 100-46-9 benzylamine 
• 74454-78-7 3-(4-hydroxyphenyl)-N-(phenylmethyl)propanamide 
• 5597-50-2 3-(4-hydroxyphenyl)propionic acid methyl ester 
• 67-56-1 methanol 
• 291313-50-3 ethyl 3-(4-acetoxyphenyl)propionate-N-benzylimidate 

Downstream Products

• 4572-26-3 1-oxaspiro[4,5]deca-6,9-dien-2,8-dione 

Relevant articles and documents

New oxidative transformations of phenolic and indolic oxazolines: An avenue to useful azaspirocyclic building-blocks

The oxidative cyclization of a phenolic amide to a spirolactam has long been regarded as an 'impossible' reaction, because exposure of the substrates to a variety of oxidants results in formation of spirolactones with consequent loss of the amine segment. We recently communicated that this heretofore unknown transformation may be achieved by oxidation of oxazoline analogues of phenolic and indolic amides. Herein, we provide full details of our work.