2979-59-1

Basic information

• Product Name: Glycine, N-benzoyl-, propyl ester
• CAS NO: 2979-59-1
• Molecular Formula: C12H15NO3
• Molecular Weight: 221.256
• Mol File: 2979-59-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Glycine, N-benzoyl-, propyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Glycine, N-benzoyl-, propyl ester(2979-59-1)
• EPA Substance Registry System: Glycine, N-benzoyl-, propyl ester(2979-59-1)

Safety Data

• Hazardous Substances Data: 2979-59-1(Hazardous Substances Data)

Upstream product

• 13049-01-9 glycine 1-propyl ester hydrochloride 
• 98-88-4 benzoyl chloride 
• 65-85-0 benzoic acid 
• 532-94-5 sodium hippurate 
• 107-08-4 1-iodo-propane 

Relevant articles and documents

Synthesis and antimicrobial activities of novel sorbic and benzoic acid amide derivatives

A series of sorbic and benzoic acid amide derivatives were synthesized by conjugating sorbic acid (SAAD, a1–a7) or benzoic acid (BAAD b1–b6) with amino acid esters and their antimicrobial activities were investigated against Escherichia coli, Bacillus subtilis and Staphylococcus aureus, mixed bacteria from rancid milk, Saccharomyces cerevisiae, and Aspergillus niger. The antimicrobial activity of sorbic acid amides was better than that of benzoic acid amides. The minimum inhibitory concentrations (MIC) of compound isopropyl N-[1-oxo-2, 4-hexadien-1-yl]-L-phenylalaninate (a7) were 0.17 mM against B. subtilis, and 0.50 mM against S. aureus, while the MIC values of sorbic acid were more than 2 mM respectively. Also, compound a7 displayed pH-independent antimicrobial activity in the range of pH 5.0–9.0 and was effective at pH 9.0. These results demonstrated that the conjugation of sorbic acid with amino acid esters led to significant improvement of in vitro antimicrobial attributes, but little effect was observed for benzoic acid amide derivatives.