1387509-46-7

Basic information

• Product Name: methyl (2-S-(methyl 2,3,4-tri-O-benzyl-6-thio-α-D-galactopyranoside)-5-N-acetyl-7,8,9-tri-O-acetyl-5-N,4-O-carbonyl-3,5-dideoxy-D-glycero-α-D-galacto-non-2-ulopyranoside)onate
• Synonyms: methyl (2-S-(methyl 2,3,4-tri-O-benzyl-6-thio-α-D-galactopyranoside)-5-N-acetyl-7,8,9-tri-O-acetyl-5-N,4-O-carbonyl-3,5-dideoxy-D-glycero-α-D-galacto-non-2-ulopyranoside)onate
• CAS NO: 1387509-46-7
• Molecular Weight: 938.016
• Mol File: 1387509-46-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: methyl (2-S-(methyl 2,3,4-tri-O-benzyl-6-thio-α-D-galactopyranoside)-5-N-acetyl-7,8,9-tri-O-acetyl-5-N,4-O-carbonyl-3,5-dideoxy-D-glycero-α-D-galacto-non-2-ulopyranoside)onate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl (2-S-(methyl 2,3,4-tri-O-benzyl-6-thio-α-D-galactopyranoside)-5-N-acetyl-7,8,9-tri-O-acetyl-5-N,4-O-carbonyl-3,5-dideoxy-D-glycero-α-D-galacto-non-2-ulopyranoside)onate(1387509-46-7)
• EPA Substance Registry System: methyl (2-S-(methyl 2,3,4-tri-O-benzyl-6-thio-α-D-galactopyranoside)-5-N-acetyl-7,8,9-tri-O-acetyl-5-N,4-O-carbonyl-3,5-dideoxy-D-glycero-α-D-galacto-non-2-ulopyranoside)onate(1387509-46-7)

Safety Data

• Hazardous Substances Data: 1387509-46-7(Hazardous Substances Data)

Upstream product

• 18311-26-7 methyl 6-O-triphenylmethyl-α-D-galactopyranoside 
• 3396-99-4 methyl α-D-galactopyranoside 
• 4356-80-3 methyl 2,3,4-tri-O-benzyl-α-D-galactopyranoside 
• 18685-19-3 methyl 2,3,4-tri-O-benzyl-6-O-trityl-α-D-galactopyranoside 
• 1387509-16-1 methyl 2,3,4-tri-O-benzyl-6-thio-α-D-galactopyranoside 
• 1261294-42-1 methyl 6-S-acetyl-2,3,4-tri-O-benzyl-6-deoxy-α-D-galactopyranoside 

Downstream Products

• 1387509-50-3 methyl (2-S-(methyl 2,3,4-tri-O-benzyl-6-thio-α-D-galactopyranoside)-5-N-acetyl-3,5-dideoxy-D-glycero-α-D-galacto-non-2-ulopyranoside)onate 

Relevant articles and documents

Highly stereoselective synthesis of primary, secondary, and tertiary α-S-sialosides under lewis acidic conditions

N-Acetyl 4-O,5-N-oxazolidinone protected sialyl phosphates of either anomeric configuration are excellent donors for the formation of α-S-sialosides at -78 °C in dichloromethane with primary, secondary, and tertiary thiols including galactose 3-, 4-, and