1172595-97-9

Basic information

• Product Name: methyl 4,7-di-O-acetyl-3,5-dideoxy-2-(4-methylphenylthio)-9-O-(methyl-4,7-di-O-acetyl-8,9-O-chloroacetyl-3,5-dideoxy-5-trifluoroacetamido-D-glycero-α-D-galacto-2-nonulopyranosylonate)-5-trifluoroacetamido-D-glycero-α-D-galacto-2-nonulopyranosidonate
• CAS NO: 1172595-97-9
• Molecular Weight: 1163.83
• Mol File: 1172595-97-9.mol

Chemical Properties

• CAS DataBase Reference: methyl 4,7-di-O-acetyl-3,5-dideoxy-2-(4-methylphenylthio)-9-O-(methyl-4,7-di-O-acetyl-8,9-O-chloroacetyl-3,5-dideoxy-5-trifluoroacetamido-D-glycero-α-D-galacto-2-nonulopyranosylonate)-5-trifluoroacetamido-D-glycero-α-D-galacto-2-nonulopyranosidonate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 4,7-di-O-acetyl-3,5-dideoxy-2-(4-methylphenylthio)-9-O-(methyl-4,7-di-O-acetyl-8,9-O-chloroacetyl-3,5-dideoxy-5-trifluoroacetamido-D-glycero-α-D-galacto-2-nonulopyranosylonate)-5-trifluoroacetamido-D-glycero-α-D-galacto-2-nonulopyranosidonate(1172595-97-9)
• EPA Substance Registry System: methyl 4,7-di-O-acetyl-3,5-dideoxy-2-(4-methylphenylthio)-9-O-(methyl-4,7-di-O-acetyl-8,9-O-chloroacetyl-3,5-dideoxy-5-trifluoroacetamido-D-glycero-α-D-galacto-2-nonulopyranosylonate)-5-trifluoroacetamido-D-glycero-α-D-galacto-2-nonulopyranosidonate(1172595-97-9)

Safety Data

• Hazardous Substances Data: 1172595-97-9(Hazardous Substances Data)

Upstream product

• 866332-36-7 (2S,4S,5R,6R)-4-Acetoxy-6-((1R,2R)-1-acetoxy-2,3-dihydroxy-propyl)-2-p-tolylsulfanyl-5-(2,2,2-trifluoro-acetylamino)-tetrahydro-pyran-2-carboxylic acid methyl ester 

Relevant articles and documents

Phosphite-based sialic acid donors in the synthesis of α(2→9) oligosialic acids

The combination of a phosphite donor and an anomeric thiocresol-protected acceptor, both with a TFA protecting group at C-5 of the sialic acid, provides good α-selectivity and yield in sialylation. Although the convergent synthetic strategy of using a phosphite disialo-donor and a disialo-acceptor assembles tetra-sialic acid efficiently, overcoming the low α-selectivity of α-anomer and purifying it remain to be achieved. Furthermore, mono- and di-sialic acids were, respectively, conjugated on carrier protein, keyhole limpet hemocyanin. The enzymatic hydrolysis method is recommended for estimating the amount of sialic acid on a protein conjugate.