219814-65-0

Basic information

• Product Name: Methyl (Phenyl 5-Acetamido-4,7,8-tri-O-acetyl-9-azido-3,5,9-trideoxy-2-thio-D-glycero-beta-D-galacto-2-nonulopyranosid)onate
• Synonyms: Methyl (Phenyl 5-Acetamido-4,7,8-tri-O-acetyl-9-azido-3,5,9-trideoxy-2-thio-D-glycero-beta-D-galacto-2-nonulopyranosid)onate;Methyl (Phenyl 5-Acetamido-4,7,8-tri-O-acetyl-9-azido-3,5,9-trideoxy-2-thio-D-glycero-β-D-galacto-2-nonulopyranosid)onate
• CAS NO: 219814-65-0
• Molecular Formula: C24H30N4O10S
• Molecular Weight: 566.58
• EINECS: -0
• Mol File: 219814-65-0.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Methyl (Phenyl 5-Acetamido-4,7,8-tri-O-acetyl-9-azido-3,5,9-trideoxy-2-thio-D-glycero-beta-D-galacto-2-nonulopyranosid)onate(CAS DataBase Reference)
• NIST Chemistry Reference: Methyl (Phenyl 5-Acetamido-4,7,8-tri-O-acetyl-9-azido-3,5,9-trideoxy-2-thio-D-glycero-beta-D-galacto-2-nonulopyranosid)onate(219814-65-0)
• EPA Substance Registry System: Methyl (Phenyl 5-Acetamido-4,7,8-tri-O-acetyl-9-azido-3,5,9-trideoxy-2-thio-D-glycero-beta-D-galacto-2-nonulopyranosid)onate(219814-65-0)

Safety Data

• Hazardous Substances Data: 219814-65-0(Hazardous Substances Data)

Upstream product

• 219814-61-6 allyl 2-acetamido-3,4-di-O-acetyl-6-azido-2-deoxy-β-D-glucopyranoside 
• 151895-54-4 allyl 2-acetamido-3,4-di-O-acetyl-2-deoxy-6-O-p-tolylsulfonyl-β-D-glucopyranoside 
• 63064-48-2 allyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranoside 
• 54400-75-8 allyl 2-acetamido-2-deoxy-β-D-glucopyranoside 
• 108-98-5 thiophenol 
• 219814-64-9 methyl (5-acetamido-4,7,8-tri-O-acetyl-9-azido-3,5,9-trideoxy-D-glycero-D-galacto-2-nonulopyranoso)onate 

Relevant articles and documents

Chemoenzymatic synthesis of an N-acetylneuraminic acid analogue having a carbamoylmethyl group at C-4 as an inhibitor of sialidase from influenza virus

5,9-Diacetamido-2,6-anhydro-O-4-carbamoylmethyl-3,5,9-trideoxy-d-glycero-d-galacto-non-2-enonic acid (1) was synthesized via a key intermediate 2 through the Neu5Ac aldolase [E.C.4.1.3.3]-catalyzed aldol reaction of 2-acetamido-2,6-dideoxy-6-azido-d-glucose with sodium pyruvate operating under alkaline conditions (pH 10.5) in order to accelerate epimerization C-2 of N-acetyl-d-glucosamine (d-GlcNAc) derivatives. Compound 1 showed inhibitory activity against sialidase. Copyright (C) 1998 Elsevier Science Ltd.