270076-02-3

Basic information

• Product Name: 5-O-dibenzylphosphono-1,2-O,O-isopropylidene-α-D-xylofuranose
• Synonyms: 5-O-dibenzylphosphono-1,2-O,O-isopropylidene-α-D-xylofuranose
• CAS NO: 270076-02-3
• Molecular Weight: 450.425
• Mol File: 270076-02-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 5-O-dibenzylphosphono-1,2-O,O-isopropylidene-α-D-xylofuranose(CAS DataBase Reference)
• NIST Chemistry Reference: 5-O-dibenzylphosphono-1,2-O,O-isopropylidene-α-D-xylofuranose(270076-02-3)
• EPA Substance Registry System: 5-O-dibenzylphosphono-1,2-O,O-isopropylidene-α-D-xylofuranose(270076-02-3)

Safety Data

• Hazardous Substances Data: 270076-02-3(Hazardous Substances Data)

Upstream product

• 538-37-4 dibenzyl phosphochloridate 
• 20031-21-4 1,2-O-isopropylidene-α-D-xylose 
• 1146540-71-7 3-O-benzoyl-5-O-dibenzylphosphono-1,2-O,O-isopropylidene-α-D-xylofuranose 

Downstream Products

• 1146540-72-8 3-O-acetyl-5-O-dibenzylphosphono-1,2-O,O-isopropylidene-α-D-xylofuranose 
• 270076-05-6 3-O-benzyl-1,2-O-isopropylidene-3-C-methyl-α-D-ribofuranose 5-dibenzylphosphate 
• 270076-08-9 2-O-benzyl-2-C-methyl-D-erythritol 4-dibenzylphosphate 
• 270076-07-8 2-O-benzyl-2-C-methyl-D-erythrose 4-dibenzylphosphate 
• 270076-04-5 1,2-O-isopropylidene-3-C-methyl-α-D-ribofuranose 5-dibenzylphosphate 
• 270076-03-4 1,2-O-isopropylidene-α-D-erythro-pentofuranose-3-ulose 5-dibenzylphosphate 

Relevant articles and documents

Chemoenzymatic synthesis of 4-diphosphocytidyl-2-C-methyl-d-erythritol: a substrate for IspE

Enantiomerically pure 2-C-methyl-d-erythritol 4-phosphate 1 (MEP) is synthesized from 1,2-O-isopropylidene-α-d-xylofuranose via facile benzylation in good yield. Subsequently, 1 is used for enzymatic synthesis of 4-diphosphocytidyl-2-C-methyl-d-erythritol

Chemical synthesis of enantiopure 2-C-methyl-D-erythritol 4-phosphate, the key intermediate in the mevalonate-independent pathway for isoprenoid biosynthesis

Optically pure 2-C-methyl-D-erythritol 4-phosphate, a key intermediate in the mevalonate-independent route for isoprenoid biosynthesis, is conveniently synthesized from 1,2-O-isopropylidene-α-D-xylofuranose, including the possibility of radiolabeling of t