1421611-55-3

Basic information

• Product Name: N-ethyl-O-benzyl-N-(β-D-galactopyranosyl(1→2)β-D-glucopyranosyl)hydroxylamine
• Synonyms: N-ethyl-O-benzyl-N-(β-D-galactopyranosyl(1→2)β-D-glucopyranosyl)hydroxylamine
• CAS NO: 1421611-55-3
• Molecular Weight: 475.493
• Mol File: 1421611-55-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-ethyl-O-benzyl-N-(β-D-galactopyranosyl(1→2)β-D-glucopyranosyl)hydroxylamine(CAS DataBase Reference)
• NIST Chemistry Reference: N-ethyl-O-benzyl-N-(β-D-galactopyranosyl(1→2)β-D-glucopyranosyl)hydroxylamine(1421611-55-3)
• EPA Substance Registry System: N-ethyl-O-benzyl-N-(β-D-galactopyranosyl(1→2)β-D-glucopyranosyl)hydroxylamine(1421611-55-3)

Safety Data

• Hazardous Substances Data: 1421611-55-3(Hazardous Substances Data)

Upstream product

• 2021-84-3 α-galactosyl fluoride 

Relevant articles and documents

Alkoxyamino glycoside acceptors for the regioselective synthesis of oligosaccharides using glycosynthases and transglycosidases

Alkoxyamino derivatives of oligosaccharides have been synthesized by enzymatic synthesis using a glycosynthase and a transglycosidase. The chemoselective assembly of unprotected oligosaccharides bearing glucose at the reducing end with N-alkyl-O-benzylhydroxylamine provides sugar derivatives that are good acceptors for enzymatic synthesis using either glycosynthase or transglycosidase. Furthermore, this method affords the possibility of controlling the regioselectivity of coupling depending on the nature of the alkoxyamino substituent and provides high-yield coupling of sugars without the need for complex protecting group chemistry.