1091627-03-0

Basic information

• Product Name: methyl phenyl 5-(N-acetylacetamido)-3,5-dideoxy-4,7,8-tri-O-propargyl-2-thio-D-glycero-α-D-galacto-non-2-(9-oxaulopyranosidonate) 1',1'-diphenyl-5-methoxysalicylic alcohol acetal
• Synonyms: methyl phenyl 5-(N-acetylacetamido)-3,5-dideoxy-4,7,8-tri-O-propargyl-2-thio-D-glycero-α-D-galacto-non-2-(9-oxaulopyranosidonate) 1',1'-diphenyl-5-methoxysalicylic alcohol acetal
• CAS NO: 1091627-03-0
• Molecular Weight: 857.978
• Mol File: 1091627-03-0.mol

Chemical Properties

• CAS DataBase Reference: methyl phenyl 5-(N-acetylacetamido)-3,5-dideoxy-4,7,8-tri-O-propargyl-2-thio-D-glycero-α-D-galacto-non-2-(9-oxaulopyranosidonate) 1',1'-diphenyl-5-methoxysalicylic alcohol acetal(CAS DataBase Reference)
• NIST Chemistry Reference: methyl phenyl 5-(N-acetylacetamido)-3,5-dideoxy-4,7,8-tri-O-propargyl-2-thio-D-glycero-α-D-galacto-non-2-(9-oxaulopyranosidonate) 1',1'-diphenyl-5-methoxysalicylic alcohol acetal(1091627-03-0)
• EPA Substance Registry System: methyl phenyl 5-(N-acetylacetamido)-3,5-dideoxy-4,7,8-tri-O-propargyl-2-thio-D-glycero-α-D-galacto-non-2-(9-oxaulopyranosidonate) 1',1'-diphenyl-5-methoxysalicylic alcohol acetal(1091627-03-0)

Safety Data

• Hazardous Substances Data: 1091627-03-0(Hazardous Substances Data)

Upstream product

• 936716-83-5 α,α-diphenyl-5-methoxysalicyl alcohol 
• 1091627-02-9 methyl phenyl 5-(N-acetylacetamido)-3,5-dideoxy-4,7,8-tri-O-propargyl-2-thio-D-glycero-α-D-galacto-non-2-(9-oxaulopyranosidonate) 

Downstream Products

• 1091627-02-9 methyl phenyl 5-(N-acetylacetamido)-3,5-dideoxy-4,7,8-tri-O-propargyl-2-thio-D-glycero-α-D-galacto-non-2-(9-oxaulopyranosidonate) 
• 1091627-04-1 methyl 5-(N-acetylacetamido)-3,5-dideoxy-4,7,8-tri-O-propargyl-2-phenylsulfonyl-D-glycero-α-D-galacto-non-2-(9-oxaulopyranosidonate) 1',1'-diphenyl-5-methoxysalicylic alcohol acetal 

Relevant articles and documents

Stereoselective synthesis of a C-linked neuraminic acid disaccharide: Potential building block for the synthesis of C-analogues of polysialic acids

(Chemical Equation Presented) C-Linked neuraminic acid disaccharide was synthesized in a diastereoselective manner from a sulfone donor and aldehyde acceptor, which was protected as a propargyl ether, through a samarium-mediated coupling reaction. The resulting disaccharide has acetal and phenyl sulfide functional groups that can be easily converted into aldehyde and phenyl sulfone groups by photolysis and oxidation reactions to serve as disaccharide acceptor and donor, respectively.