64410-44-2

Basic information

• Product Name: N-(tert-butoxycarbonyl)-D-alanylglycine benzyl ester
• Synonyms: N-(tert-butoxycarbonyl)-D-alanylglycine benzyl ester
• CAS NO: 64410-44-2
• Molecular Weight: 336.388
• Mol File: 64410-44-2.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: N-(tert-butoxycarbonyl)-D-alanylglycine benzyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: N-(tert-butoxycarbonyl)-D-alanylglycine benzyl ester(64410-44-2)
• EPA Substance Registry System: N-(tert-butoxycarbonyl)-D-alanylglycine benzyl ester(64410-44-2)

Safety Data

• Hazardous Substances Data: 64410-44-2(Hazardous Substances Data)

Upstream product

• 34404-33-6 N-tertiarybutoxycarbonyl-D-alanine N-hydroxysuccinimide ester 
• 1738-76-7 glycine benzyl ester p-toluenesulfonic acid salt 
• 3744-87-4 Boc-(R)-Ala 
• 2462-31-9 benzyl 2-aminoacetate hydrochloride 

Downstream Products

• 79807-16-2 t-butoxycarbonyl-D-alanyl-glycyl-L-phenylalanyl-(Z)-α,β-dehydroleucine benzyl ester 
• 80458-15-7 L-tyrocyl-D-alanyl-glycyl-L-phenylalanyl-(Z)-α,β-dehydroleucine 
• 74814-12-3 H-D-Ala-Gly-Phe-D-Leu-OBzl*HCl 
• 74814-14-5 Boc-Tyr(αMe)-D-Ala-Gly-Phe-D-Leu-OH 
• 74814-13-4 Boc-Glu(OEt)-D-Ala-Gly-Phe-D-Leu-OH 
• 74814-09-8 Boc-Tyr-D-Ala-Gly-Phe(αMe)-Val-OH 
• 74814-17-8 Boc-Tyr-D-Ala-Gly-Cha-D-Leu-OH 
• 74814-11-2 Boc-D-Ala-Gly-Phe-D-Leu-OBzl 
• 74814-28-1 Boc-Tyr(OH)-D-Ala-Gly-1-aminoindan 
• 74814-29-2 Boc-Tyr(OH)-D-Ala-Gly-2-aminoindan 
• 74814-30-5 Boc-Tyr(OH)-D-Ala-Gly-2-phenylethylamine 
• 74814-31-6 Boc-Tyr(OH)-D-Ala-Gly-benzylamine 
• 74814-33-8 Boc-Tyr(OH)-D-Ala-Gly-(aminomethyl)cyclobutane 
• 74814-32-7 Boc-Tyr(OH)-D-Ala-Gly-(aminomethyl)cyclopropane 

Relevant articles and documents

Antiviral Immunotropic Agent for the Treatment of Acute Respiratory Viral Infections

The proposed methods of treatment pertain to medicine, in particular pharmacology, and concerns the application of a nasal medicinal composition containing hexapeptide tyrosyl-D-alanyl-glycyl-phenylalanyl-leucyl-arginine or its pharmaceutically acceptable

Amino acids and peptides. XXIV. Preparation and antinociceptive effect of [D-Ala2, (N-Me)Phe4]enkephalin analog-poly(ethylene glycol) hybrids

Hybrids of amino-poly(ethylene glycol) (aPEG) and [D-Ala2,(N-Me)Phe4]enkephalin analogs, H-Tyr-D-Ala-Gly-(Me)Phe-aPEG, H-Tyr-D-Ala-Gly-(Me)Phe-Leu-aPEG and H-Tyr-D-Ala-Gly-(Me)Phe-D-Leu-aPEG, were prepared by the solution method and

Novel Analogues of Enkephalin: Identification of Functional Groups Required for Biological Activity

Novel tri- and tetrapeptide analogues of enkephalin, in conjunction with earlier structure-activity data, confirm that chemical substituents present in the first and fourth residues of enkephalin are required for in vitro biological activity.A class of ar