918161-13-4

Basic information

• Product Name: acetic acid (R)-1-(4-methoxy-benzylcarbamoyl)-2-phenyl-ethyl ester
• Synonyms: acetic acid (R)-1-(4-methoxy-benzylcarbamoyl)-2-phenyl-ethyl ester
• CAS NO: 918161-13-4
• Molecular Weight: 327.38
• Mol File: 918161-13-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: acetic acid (R)-1-(4-methoxy-benzylcarbamoyl)-2-phenyl-ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: acetic acid (R)-1-(4-methoxy-benzylcarbamoyl)-2-phenyl-ethyl ester(918161-13-4)
• EPA Substance Registry System: acetic acid (R)-1-(4-methoxy-benzylcarbamoyl)-2-phenyl-ethyl ester(918161-13-4)

Safety Data

• Hazardous Substances Data: 918161-13-4(Hazardous Substances Data)

Upstream product

• 918161-07-6 rac-acetic acid 1-(4-methoxy-benzylcarbamoyl)-2-phenyl-ethyl ester 
• 918161-15-6 acetic acid (S)-1-(4-methoxy-benzylcarbamoyl)-2-phenyl-ethyl ester 
• 918161-14-5 (R)-2-hydroxy-N-(4-methoxybenzyl)-3-phenyl-propionamide 
• 918161-08-7 (S)-2-hydroxy-N-(4-methoxybenzyl)-3-phenyl-propionamide 
• 918161-11-2 toluene-4-sulfonic acid (S)-1-(4-methoxy-benzylcarbamoyl)-2-phenyl-ethyl ester 
• 3396-11-0 cesium acetate 

Downstream Products

• 918161-14-5 (R)-2-hydroxy-N-(4-methoxybenzyl)-3-phenyl-propionamide 
• 918161-08-7 (S)-2-hydroxy-N-(4-methoxybenzyl)-3-phenyl-propionamide 
• 918161-10-1 (R)-2-amino-N-(4-methoxy-benzyl)-3-phenyl-propionamide 
• 918161-12-3 (R)-2-azido-N-(4-methoxybenzyl)-3-phenyl-propionamide 
• 918161-09-8 methanesulfonic acid (S)-1-(4-methoxy-benzylcarbamoyl)-2-phenyl-ethyl ester 
• 918161-15-6 acetic acid (S)-1-(4-methoxy-benzylcarbamoyl)-2-phenyl-ethyl ester 
• 673-06-3 D-(R)-phenylalanine 
• 2448-45-5 Cbz-D-Phe 
• 28069-46-7 D-phenylalanine hydrochloride 

Relevant articles and documents

Studies on the application of the Passerini reaction and enzymatic procedures to the synthesis of tripeptide mimetics

A new, efficient method for the multicomponent synthesis of tripeptide mimetics is presented. Simple, chemoenzymatic transformations of Passerini reaction products enable the introduction of varied amino acid moieties into the tripeptide scaffold, with co