4252-32-8

Basic information

• Product Name: BenzeneacetaMide, N-forMyl-
• Synonyms: BenzeneacetaMide, N-forMyl-;N-Formyl-2-phenylacetamide
• CAS NO: 4252-32-8
• Molecular Formula: C₉H₉NO₂
• Molecular Weight: 163.17326
• Mol File: 4252-32-8.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: BenzeneacetaMide, N-forMyl-(CAS DataBase Reference)
• NIST Chemistry Reference: BenzeneacetaMide, N-forMyl-(4252-32-8)
• EPA Substance Registry System: BenzeneacetaMide, N-forMyl-(4252-32-8)

Safety Data

• Hazardous Substances Data: 4252-32-8(Hazardous Substances Data)

Upstream product

• 15500-60-4 N,N-bis(trimethylsilyl)formamide 
• 103-80-0 phenylacetyl chloride 
• 500-98-1 phenylacetylglycine 

Downstream Products

• 7651-81-2 3-Hydroxyisoquinoline 

Relevant articles and documents

Oxidative photo-decarboxylation in the presence of mesoporous silicas

FSM-16, a mesoporous silica, was found to catalyze oxidative photo-decarboxylation of α-hydroxy carboxylic acid, phenyl acetic acid derivatives and N-acyl-protected α-amino acids to afford the corresponding carbonyl compounds. Furthermore, FSM-16 proved to be re-usable by re-calcination at 450°C after the reaction.

Irreversible Inhibition of Mammalian and Insect Peptidylglycine &α-Hydroxylating Monooxygenases (PHMs), Peptide Amidating Enzymes, by N-Formyl Amides

A series of N-formyl amides were synthesized by condensation of N,N-bis(trimethylsilyl)formamide with acid chlorides (59-90percent yields), or by reaction of hydroxyglycyl peptides with 90percent hydrogen peroxide (45percent yield); a number of N-formyl amides which bear a phenyl substituent are mechanism-based irreversible inactivators of peptidylglycine α-hydroxylating monooxygenases purified from pig pituitary and from honeybee heads.