3916-37-8

Basic information

• Product Name: N-(N-benzyloxycarbonyl-glycyl)-glycine-(4-nitro-benzyl ester)
• Synonyms: N-(N-benzyloxycarbonyl-glycyl)-glycine-(4-nitro-benzyl ester)
• CAS NO: 3916-37-8
• Molecular Weight: 401.376
• Mol File: 3916-37-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-(N-benzyloxycarbonyl-glycyl)-glycine-(4-nitro-benzyl ester)(CAS DataBase Reference)
• NIST Chemistry Reference: N-(N-benzyloxycarbonyl-glycyl)-glycine-(4-nitro-benzyl ester)(3916-37-8)
• EPA Substance Registry System: N-(N-benzyloxycarbonyl-glycyl)-glycine-(4-nitro-benzyl ester)(3916-37-8)

Safety Data

• Hazardous Substances Data: 3916-37-8(Hazardous Substances Data)

Upstream product

• 619-73-8 4-nitrobenzyl chloride 
• 1138-80-3 N-(Benzyloxycarbonyl)glycine 
• 5680-83-1 N-(benzyloxycarbonyl)glycine hydrazide 
• 5680-82-0 PNB-glycinate hydrobromide 
• 2566-19-0 CbzGlyGly 
• 100-11-8 1-bromomethyl-4-nitro-benzene 
• 7352-39-8 N-Carbonyl-glycin-(4-nitro-benzylester) 
• 7352-64-9 glycine 4-nitrobenzyl ester 

Downstream Products

• 77217-26-6 Glycylglycin-p-nitrobenzylester 
• 556-50-3 glycylglycine 

Relevant articles and documents

Vibrational spectra of N-acetylglycine oligomers. Part 2. - Raman scattering study of selectively C-deuteriated oligomers with polyglycine I- and II-type structures

Selectively C-deuteriated N-acetylglycine trimer and tetramer acid types have been synthesized, and their two crystalline modifications, solid-A and solid-B [which correspond in structure to polyglycine (PG) II and I, respectively] have been prepared. Raman scattering spectra have been measured for a series of these glycine oligomers, and the CH2- and CD2-characteristic modes have been investigated in detail. Assignment of the CH2-characteristic bands to each CH2 group in the oligomers has been carried out successfully. In particular, the results obtained from the CD2 stretch region show that N- and C-terminal glycine residues for the PGI- and PGII-type trimers and tetramers are all in very similar environments and that the glycine residues which are sandwiched between the two terminal residues are also in a similar environment for both the trimers and the tetramers.