949159-01-7

Basic information

• Product Name: C₄₅H₅₀O₁₃
• Synonyms: C₄₅H₅₀O₁₃
• CAS NO: 949159-01-7
• Molecular Weight: 798.884
• Mol File: 949159-01-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₄₅H₅₀O₁₃(CAS DataBase Reference)
• NIST Chemistry Reference: C₄₅H₅₀O₁₃(949159-01-7)
• EPA Substance Registry System: C₄₅H₅₀O₁₃(949159-01-7)

Safety Data

• Hazardous Substances Data: 949159-01-7(Hazardous Substances Data)

Upstream product

• 81600-93-3 allyl 4,6-di-O-benzylidene-α-D-mannopyranoside 
• 41308-76-3 allyl α-D-mannopyranoside 
• 1125-88-8 benzaldehyde dimethyl acetal 
• 7296-15-3 alpha-D-mannopyranoside 
• 949158-96-7 C₂₄H₂₈O₇ 
• 949159-32-4 C₂₄H₂₆O₇ 
• 949158-99-0 C₄₄H₅₇O₁₀SiP 
• 949158-97-8 C₃₃H₄₈O₇Si 
• 949159-00-6 C₅₄H₇₀O₁₃Si 

Downstream Products

• 949159-04-0 C₉₆H₁₁₄O₂₅Si 

Relevant articles and documents

Highly stereoselective and iterative synthesis of α-(1→4)-linked polysaccharides composed of 3-O-methyl-D-mannose

A second-generation synthesis of synthetic 3-O-methyl-D-mannose-containing polysaccharides (sMMPs) is reported. The glycosidation of donor B and acceptor C, prepared from a common precursor A in two and one steps, respectively, is effected by t-butyldimethylsilyl trifluoromethanesulfonate to furnish only the desired α-anomer D in high yields. Unlike the first-generation synthesis, this synthesis gives the desired product free from contamination of scrambling products. A three-step protocol is used to deprotect D to furnish sMMPs.