100906-46-5

Basic information

• Product Name: [(4'S,5'S)-5'-(benzyloxy)-2',2'-dimethyl-1',3'-dioxan-4'-yl]methanol
• Synonyms: [(4'S,5'S)-5'-(benzyloxy)-2',2'-dimethyl-1',3'-dioxan-4'-yl]methanol
• CAS NO: 100906-46-5
• Molecular Weight: 252.31
• Mol File: 100906-46-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: [(4'S,5'S)-5'-(benzyloxy)-2',2'-dimethyl-1',3'-dioxan-4'-yl]methanol(CAS DataBase Reference)
• NIST Chemistry Reference: [(4'S,5'S)-5'-(benzyloxy)-2',2'-dimethyl-1',3'-dioxan-4'-yl]methanol(100906-46-5)
• EPA Substance Registry System: [(4'S,5'S)-5'-(benzyloxy)-2',2'-dimethyl-1',3'-dioxan-4'-yl]methanol(100906-46-5)

Safety Data

• Hazardous Substances Data: 100906-46-5(Hazardous Substances Data)

Upstream product

• 116-11-0 2-Methoxypropene 
• 84379-51-1 2-O-benzyl-L-threitol 
• 38270-72-3 dimethyl 2,3-O-benzylidene-L-tartrate 
• 100-52-7 benzaldehyde 
• 38270-70-1 4,5-trans-bis(methoxycarbonyl)-2-phenyl-1,3-dioxolan 

Downstream Products

• 1198777-74-0 {[(4S,5S)-5-(benzyloxy)-2,2-dimethyl-1,3-dioxan-4-yl]methoxy}(tert-butyl)diphenylsilane 

Relevant articles and documents

Total synthesis of pachastrissamine together with its 4-epi-congener via [3,3]-sigmatropic rearrangements and antiproliferative/cytotoxic evaluation Dedicated to Associated Professor Ladislav Knieo on the occasion of his 70th birthday

Synthesis of the HCl salts of two anhydrophytosphingosines, jaspine B (1) and its 4-epi-congener 5 from easily available dimethyl l-tartrate and/or l-arabinose, is described. The key transformations are the efficient incorporation of a chiral amino group

THE USE OF L-TARTARIC ACID IN THE SYNTHESIS OF ENANTIOMERICALLY PURE COMPOUNDS: SYNTHESIS OF 4-O-BENZYL-2,3-DIDEOXI-L-THREO-HEX-2-ENONO-1,5-LACTONE

The title compound was obtained through a seven steps sequence and using -dimethyl L-tartrate as the starting material (30percent overall yield).The system 2,3-dideoxy-L-threo-hex-2-enono-1,5-lactone is present in several natural compounds.