2543-27-3

Basic information

• Product Name: Glycine, N-[N-[(phenylmethoxy)carbonyl]-L-seryl]-, phenylmethyl ester
• CAS NO: 2543-27-3
• Molecular Formula: C20H22N2O6
• Molecular Weight: 386.404
• Mol File: 2543-27-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Glycine, N-[N-[(phenylmethoxy)carbonyl]-L-seryl]-, phenylmethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Glycine, N-[N-[(phenylmethoxy)carbonyl]-L-seryl]-, phenylmethyl ester(2543-27-3)
• EPA Substance Registry System: Glycine, N-[N-[(phenylmethoxy)carbonyl]-L-seryl]-, phenylmethyl ester(2543-27-3)

Safety Data

• Hazardous Substances Data: 2543-27-3(Hazardous Substances Data)

Upstream product

• 1676-81-9 N-benzyloxycarbonyl-L-serine methyl ester 
• 1145-80-8 N-(benzyloxycarbonyl)-L-serine 
• 1738-76-7 glycine benzyl ester p-toluenesulfonic acid salt 
• 1738-68-7 Gly-OBz 
• 26582-86-5 benzyl (1S)-2-hydrazino-1-(hydroxymethyl)-2-oxoethylcarbamate 

Downstream Products

• 162355-80-8 N-benzyloxycarbonyl-O-4)-(3-O-acetyl-β-D-xylopyranosyl)>-L-serylglycine benzyl ester 
• 162355-77-3 N-benzyloxycarbonyl-O-4)-β-D-xylopyranosyl>-L-serylglycine benzyl ester 
• 162355-76-2 N-benzyloxycarbonyl-O-4)-(2,3-O-isopropylidene-β-D-xylopyranosyl)>-L-serylglycine benzyl ester 
• 162355-75-1 N-benzyloxycarbonyl-O-(2,3-O-isopropylidene-β-D-xylopyranosyl)-L-serylglycine benzyl ester 
• 162355-73-9 N-benzyloxycarbonyl-O-β-D-xylopyranosyl-L-serylglycine benzyl ester 
• 162355-72-8 N-benzyloxycarbonyl-O-(2,3,4-tri-O-chloroacetyl-β-D-xylopyranosyl)-L-serylglycine benzyl ester 
• 138479-90-0 N-(Benzyloxycarbonyl)-O-<2,3-di-O-benzoyl-4-O-(2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl)-β-D-xylopyranosyl>-L-seryl-glycine benzyl ester 
• 82213-72-7 N-(O-acetyl-N-benzyloxycarbonyl-L-seryl)-glycine benzyl ester 
• 6402-93-3 H-Ser-Gly-OBzl 
• 687-63-8 L-Ser-Gly 

Relevant articles and documents

Synthesis of glycopeptides from the carbohydrate-protein linkage region of proteoglycans

2,3,4,6-Tetra-O-benzoyl-α-D-galactopyranosyl trichloroacetimidate was condensed with benzyl 2,3-O-isopropylidene-β-D-xylopyranoside to give the corresponding β-(1->4)-linked disaccharide derivative, which was transformed into 2,3-di-O-benzoyl-4-O-(2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl)-α-D-xylopyranosyl trichloroacetimidate.This glycosyl donor was condensed with a set of selectively C,N-protected L-seryl-glycine dipeptide units.Selective deblocking at the C- or N-termini of the glycosylated or non-glycosylated dipeptide segments, and coupling using the mixed-anhydride procedure allowed the construction in high yield of partially or fully glycosylated oligopeptides from the carbohydrate-protein linkage region of proteoglycans.