87604-55-5

Basic information

• Product Name: (2R,3S)-3-O-benzylbutane-1,2,3-triol
• Synonyms: (2R,3S)-3-O-benzylbutane-1,2,3-triol
• CAS NO: 87604-55-5
• Molecular Weight: 196.246
• Mol File: 87604-55-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (2R,3S)-3-O-benzylbutane-1,2,3-triol(CAS DataBase Reference)
• NIST Chemistry Reference: (2R,3S)-3-O-benzylbutane-1,2,3-triol(87604-55-5)
• EPA Substance Registry System: (2R,3S)-3-O-benzylbutane-1,2,3-triol(87604-55-5)

Safety Data

• Hazardous Substances Data: 87604-55-5(Hazardous Substances Data)

Upstream product

• 100-39-0 benzyl bromide 
• 100-44-7 benzyl chloride 
• 87604-49-7 (2R,3S)-3-O-benzyl-1,2-O-isopropylidenebutane-1,2,3-triol 

Downstream Products

• 81445-44-5 (S)-2-(benzyloxy)propanal 
• 114185-04-5 (2R,3S)-3-(benzyloxy)-1,2-epoxybutane 
• 33106-32-0 (S)-2-(benzyloxy)propanoic acid 
• 33106-64-8 (S)-2-(benzyloxy)propan-1-ol 
• 114185-05-6 1,3-O-dibenzylbutane-1,2R,3S-triol 
• 114185-06-7 (2R,3S)-2,3-di-O-benzylbutane-1,2,3-triol 
• 114185-03-4 (2R,3S)-3-O-benzyl-1,2-O-benzylidenebutane-1,2,3-triol 

Relevant articles and documents

Synthesis of the C-8-C-24 Fragment of Maltepolide C by Using a Tandem Dihydroxylation/SN2 Cyclization Sequence

A highly stereoselective synthesis of the C-8-C-24 fragment of maltepolide C has been achieved in a convergent and efficient manner by utilizing a tandem Sharpless asymmetric dihydroxylation (SAD)/SN2 cyclization reaction sequence as the key st

ON THE STERIC COURSE OF THE ADDITION OF SOME ORGANOMETALLIC REAGENTS TO (R)-2,3-ISOPROPYLIDENE GLYCERALDEHYDE. SYNTHESIS OF OPTICALLY ACTIVE α-BENZYLOXY ALDEHYDES, ALCOHOLS, CARBOXYLIC ACIDS AND 1,2-DIOLS.

Organo-titanium and organo-zinc reagents were added stereoselectively to (R)-2,3-isopropylidene glyceraldehyde (1) to give the alcohols 2/3, which were converted into the optically active derivatives 4-11.