221278-44-0

Basic information

• Product Name: 1,5-anhydro-6-O-monomethoxytrityl-3-O-tert-butyldimethylsilyl-4-deoxy-D-glucitol
• CAS NO: 221278-44-0
• Molecular Weight: 534.768
• Mol File: 221278-44-0.mol

Chemical Properties

• CAS DataBase Reference: 1,5-anhydro-6-O-monomethoxytrityl-3-O-tert-butyldimethylsilyl-4-deoxy-D-glucitol(CAS DataBase Reference)
• NIST Chemistry Reference: 1,5-anhydro-6-O-monomethoxytrityl-3-O-tert-butyldimethylsilyl-4-deoxy-D-glucitol(221278-44-0)
• EPA Substance Registry System: 1,5-anhydro-6-O-monomethoxytrityl-3-O-tert-butyldimethylsilyl-4-deoxy-D-glucitol(221278-44-0)

Safety Data

• Hazardous Substances Data: 221278-44-0(Hazardous Substances Data)

Upstream product

• 221278-41-7 1,5-anhydro-6-O-monomethoxytrityl-2,3-O-bis-pivaloyl-D-glucitol 
• 221278-42-8 1,5-anhydro-6-O-monomethoxytrityl-2,3-bis-O-pivaloyl-4-deoxy-D-glucitol 
• 221278-40-6 1,5-anhydro-2,3-O-bis-pivaloyl-D-glucitol 
• 65190-39-8 (4aR,7S,8R,8aS)-2-phenylhexahydropyrano[3,2-d][1,3]dioxine-7,8-diol 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 221278-43-9 1,5-anhydro-6-O-monomethoxytrityl-4-deoxy-D-glucitol 

Downstream Products

• 221278-46-2 1,5-anhydro-6-O-monomethoxytrityl-3-O-tert-butyldimethylsilyl-2-(adenin-9-yl)-2,4-dideoxy-D-mannitol 

Relevant articles and documents

Synthesis and conformational analysis of 1,5-anhydro-2,4 dideoxy-D- mannitol nucleosides

1,5-Anhydro-4,6-O-benzylidene-D-glucitol was used as starting material for the synthesis of 1,5-anhydro-2,4-dideoxy-D-mannitol nucleosides with an adenine and uracil base moiety. The compound with a purine base was obtained by direct nucleophilic substitution of a triflate. The pyrimidine nucleoside could be obtained by epoxide opening followed by inversion of configuration at the 3'-position. Both nucleosides adopt a C1 conformation with an axial base moiety.