87423-40-3

Basic information

• Product Name: Glycine, N-[N-[N-[(1,1-dimethylethoxy)carbonyl]-O-(phenylmethyl)-L-tyrosyl]glycyl] -, ethyl ester
• CAS NO: 87423-40-3
• Molecular Formula: C27H35N3O7
• Molecular Weight: 513.591
• Mol File: 87423-40-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Glycine, N-[N-[N-[(1,1-dimethylethoxy)carbonyl]-O-(phenylmethyl)-L-tyrosyl]glycyl] -, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Glycine, N-[N-[N-[(1,1-dimethylethoxy)carbonyl]-O-(phenylmethyl)-L-tyrosyl]glycyl] -, ethyl ester(87423-40-3)
• EPA Substance Registry System: Glycine, N-[N-[N-[(1,1-dimethylethoxy)carbonyl]-O-(phenylmethyl)-L-tyrosyl]glycyl] -, ethyl ester(87423-40-3)

Safety Data

• Hazardous Substances Data: 87423-40-3(Hazardous Substances Data)

Upstream product

• 25438-03-3 N-tert-butoxycarbonylglycylglycine ethyl ester 
• 2130-96-3 O-benzyl-N-tert-butoxycarbonyl-L-tyrosine 
• 2087-41-4 glycyl glycine ethyl ester hydrochloride 
• 623-33-6 glycine ethyl ester hydrochloride 
• 41296-45-1 N-Boc-Tyr(Bn)-Gly-OH 

Downstream Products

• 88621-28-7 H-Tyr-Gly-Gly-Phet-Leu-OH 
• 88621-27-6 Boc-Tyr(Bzl)-Gly-Gly-Phet-Leu-OBzl 
• 69472-91-9 tert-Butoxycarbonyl-O-benzyl-L-tyrosyl-glycyl-glycin 
• 81638-88-2 amide of N-t-butyloxycarbonyl-O-benzyl-L-tyrosylglycylglycyl-L-phenylalanyl-L-leucine 

Relevant articles and documents

A new coupling reagent for peptide synthesis. Benzotriazolvyloxy-bis (pyrroltdino) -carbonium hexaflouorophosphate (BBC)

Benzotriazolyloxy-bis(pyrrolidino)-carbonium hexa- fluorophosphate (BBC) is found to be a new excellent coupling reagent devoid of cytotoxic by-product instead of HBTU and BOP. It has been applied in the solution and solid phase peptide synthesis.

Studies on Amino Acids and Peptides. Part 6. Methods for Introducing Thioamide Bonds into the Peptide Backbone: Synthesis of the Four Monothio Analogues of Leucine Enkephalin

A methodology for preparing peptide analogues in which a thioamide bond replaces the normal amide bond is described.Thus, the synthesis of the three leucine enkephalin analogues 4>-, 2>-, and 1>-leucine enke