60566-43-0

Basic information

• Product Name: Glycine, N-[N-[N-[(1,1-dimethylethoxy)carbonyl]-L-tyrosyl]glycyl]-, phenylmethyl ester
• CAS NO: 60566-43-0
• Molecular Formula: C25H31N3O7
• Molecular Weight: 485.537
• Mol File: 60566-43-0.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Glycine, N-[N-[N-[(1,1-dimethylethoxy)carbonyl]-L-tyrosyl]glycyl]-, phenylmethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Glycine, N-[N-[N-[(1,1-dimethylethoxy)carbonyl]-L-tyrosyl]glycyl]-, phenylmethyl ester(60566-43-0)
• EPA Substance Registry System: Glycine, N-[N-[N-[(1,1-dimethylethoxy)carbonyl]-L-tyrosyl]glycyl]-, phenylmethyl ester(60566-43-0)

Safety Data

• Hazardous Substances Data: 60566-43-0(Hazardous Substances Data)

Upstream product

• 7797-34-4 benzylglycylglycinate hydrochloride 
• 31972-51-7 N-(tert-butoxycarbonyl)glycylglycine benzyl ester 
• 2462-31-9 benzyl 2-aminoacetate hydrochloride 
• 1842-55-3 glycylglycine benzyl ester 
• 3978-80-1 Boc-Tyr-OH 

Downstream Products

• 59481-76-4 tert-butoxycarbonyl-L-tyrosyl-glycyl-glycine 
• 88556-53-0 Boc-Tyr-Gly-Gly-NHNH₂ 
• 21778-69-8 tyrosylglycylglycine 
• 68835-86-9 Boc-L-Tyr-Gly-Gly-L-Phe-L-Leu-OMe 
• 84047-92-7 Boc-Tyr-Gly-Gly-Phe-Leu-NHNH₂ 
• 58822-25-6 Leu-enkephalin 
• 64963-27-5 N-tert-butyloxycarbonyl-L-tyrosyl-glycyl-glycyl-L-phenylalanyl-L-leucine 
• 66831-30-9 Tert-butyloxycarbonyltyrosyl-glycyl-glycyl-phenylalanyl-leucine Benzyl Ester 
• 98317-57-8 Tert-butyloxycarbonylmethionyl-tyrosyl-glycyl-glycyl-phenylalanyl-leucine 
• 98317-56-7 Tert-butyloxycarbonyltyrosyl-glycyl-glycyl-phenylalanyl-leucyl-methionine Methyl Ester 
• 98317-58-9 (S)-6-Amino-2-{(S)-2-[(S)-2-(2-{2-[(S)-2-tert-butoxycarbonylamino-3-(4-hydroxy-phenyl)-propionylamino]-acetylamino}-acetylamino)-3-phenyl-propionylamino]-4-methyl-pentanoylamino}-hexanoic acid 
• 98317-55-6 Tert-butyloxycarbonyltyrosyl-glycyl-glycyl-phenylalanyl-leucyl-ε-benzyloxycarbonyllysine Benzyl Ester 
• 98317-53-4 Tyrosyl-glycyl-glycyl-phenylalanyl-leucyl-methionine 
• 83404-43-7 Tyrosyl-glycyl-glycyl-phenylalanyl-leucyl-lysine 

Relevant articles and documents

Thioamides: Synthesis, stability, and immunological activities of thioanalogues of imreg. Preparation of new thioacylating agents using fluorobenzimidazolone derivatives

Imreg (Tyr1-Gly2-Gly3) is a well-known immunostimulant. However, it possesses a short half-life. Stabilized analogues of Imreg were prepared by a regioselective insertion in which peptide bonds at position 1,2 or 2,3 were

Preparation and properties of three analogues of [5-leucine]enkephalin, substrates for enzyme conversion studies

-