24250-70-2

Basic information

• Product Name: N-(1-carbamoylethyl)benzamide
• Synonyms: N-(1-carbamoylethyl)benzamide
• CAS NO: 24250-70-2
• Molecular Formula: C₁₀H₁₂N₂O₂
• Molecular Weight: 192.2145
• Mol File: 24250-70-2.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 476.4°Cat760mmHg
• Flash Point: 241.9°C
• Appearance: /
• Density: 1.172g/cm³
• Vapor Pressure: 3.07E-09mmHg at 25°C
• Refractive Index: 1.555
• CAS DataBase Reference: N-(1-carbamoylethyl)benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(1-carbamoylethyl)benzamide(24250-70-2)
• EPA Substance Registry System: N-(1-carbamoylethyl)benzamide(24250-70-2)

Safety Data

• Hazardous Substances Data: 24250-70-2(Hazardous Substances Data)

Usage

InChI:InChI=1/C10H12N2O2/c1-7(9(11)13)12-10(14)8-5-3-2-4-6-8/h2-7H,1H3,(H2,11,13)(H,12,14)

Upstream product

• 5446-46-8 ethyl 2-(benzoylamino)propanoate 
• 51127-13-0 2-phenyl-4-methyl-4H-oxazolin-5-one 
• 60-29-7 diethyl ether 
• 7664-41-7 ammonia 
• 2198-64-3 N-Benzoylalanine 
• 7244-67-9 methyl N-benzoylalaninate 
• 397851-05-7 N-Benzoylalanyl chloride 

Downstream Products

• 7244-67-9 methyl N-benzoylalaninate 
• 142066-06-6 N-Benzoyl-DL-thioalanin-O-ethylester 

Relevant articles and documents

Glycine-selective α-carbon-nitrogen bond cleavage of dipeptides by nickel peroxide

Nickel peroxide selectively cleaves the α-carbon-nitrogen bond of glycine residues in dipeptide derivatives to give the corresponding amides. The glycine selectivity is attributable to preferential complexation of the reactant residue to nickel peroxide and subsequent reaction via a stable α-centered glycyl radical. The oxidation process serves as a chemical model for peptidylglycine α-amidating monooxygenase (PAM) and, in addition, may have potential for the synthesis of α,β-didehydro amino acid residues within peptides.