343925-48-4

Basic information

• Product Name: ((3aS,5R,6S,6aS)-6-Benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-ylmethoxy)-tert-butyl-diphenyl-silane
• Synonyms: ((3aS,5R,6S,6aS)-6-Benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-ylmethoxy)-tert-butyl-diphenyl-silane
• CAS NO: 343925-48-4
• Molecular Weight: 518.725
• Mol File: 343925-48-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: ((3aS,5R,6S,6aS)-6-Benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-ylmethoxy)-tert-butyl-diphenyl-silane(CAS DataBase Reference)
• NIST Chemistry Reference: ((3aS,5R,6S,6aS)-6-Benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-ylmethoxy)-tert-butyl-diphenyl-silane(343925-48-4)
• EPA Substance Registry System: ((3aS,5R,6S,6aS)-6-Benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-ylmethoxy)-tert-butyl-diphenyl-silane(343925-48-4)

Safety Data

• Hazardous Substances Data: 343925-48-4(Hazardous Substances Data)

Upstream product

• 100-39-0 benzyl bromide 
• 133048-89-2 5-O-tert-butyldiphenylsilyl-1,2-O-isopropylidene-β-D-lyxofuranose 
• 162517-90-0 5-O-(tert-butyldiphenylsilyl)-D-arabinose diethyldithioacetal 
• 114738-04-4 (3aS,5R,6R,6aS)-5-(((tert-butyldiphenylsilyl)oxy)methyl)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-6-ol 
• 172751-32-5 5-O-(tert-butyldiphenylsilyl)-1,2-O-isopropylidene-β-D-threo-pentofuranose-3-ulose 
• 1941-50-0 D-arabinose diethyl dithioacetal 
• 10323-20-3 D-Arabinose 

Downstream Products

• 343925-50-8 (2R,3R)-2-(benzyloxy)-4-{[tert-butyl(diphenyl)silyl]oxy}butane-1,3 diol 
• 206983-88-2 1,2,3-O-tribenzyl-D-threitol 
• 206983-89-3 3,4,5-O-tribenzyl-1-deoxy-D-xylulose 

Relevant articles and documents

Elucidation of the 2-C-methyl-D-erythritol 4-phosphate pathway for isoprenoid biosynthesis: Straightforward syntheses of enantiopure 1-deoxy-D-xylulose from pentose derivatives

Optically pure 1-deoxy-D-xylulose, a key metabolite for feeding experiments in the methylerythritol phosphate pathway for isoprenoid biosynthesis, is conveniently synthesised from 1,2-O-isopropylidene-α-D-xylofuranose or from D-arabinose. This renders lab