82659-86-7

Basic information

• Product Name: (S)-(+)-1,3-butanediol 1-benzoate
• Synonyms: (S)-(+)-1,3-butanediol 1-benzoate
• CAS NO: 82659-86-7
• Molecular Weight: 194.23
• Mol File: 82659-86-7.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: (S)-(+)-1,3-butanediol 1-benzoate(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-(+)-1,3-butanediol 1-benzoate(82659-86-7)
• EPA Substance Registry System: (S)-(+)-1,3-butanediol 1-benzoate(82659-86-7)

Safety Data

• Hazardous Substances Data: 82659-86-7(Hazardous Substances Data)

Upstream product

• 339204-85-2 Benzoic acid (R)-3-(tetrahydro-pyran-2-yloxy)-butyl ester 
• 6290-03-5 (R)-butane-1,3-diol 
• 98-88-4 benzoyl chloride 
• 24621-61-2 1,3-butanediol 

Downstream Products

• 1379680-90-6 (R)-3-(tert-butyldimethylsilyloxy)butyl benzoate 
• 135081-58-2 C₁₇H₁₈O₄⁽¹⁸⁾OS 
• 135081-59-3 C₁₇H₁₈O₄⁽¹⁸⁾OS 
• 129991-11-3 (S)-(+)-3-<(N-methyl-N-trifluoromethanesulfonyl)amino>-1-butanol benzoate 
• 902128-54-5 benzoic acid 3-(tert-butyl-dimethyl-silanyloxy)-butyl ester 
• 24621-61-2 1,3-butanediol 
• 129990-96-1 (R)-(-)-3-<(N-methyl-N-trifluoromethanesulfonyl)amino>-1-butanol benzoate 

Relevant articles and documents

Stereoselective synthesis of ophiocerin B

A stereoselective total synthesis of ophiocerin B is reported by asymmetric synthesis, starting from L-malic acid. Of the three stereogenic centers, the vic-diols C-3, C-4 were obtained by Sharpless asymmetric dihydroxylation. ARKAT-USA, Inc.

Enantioselective total synthesis of aigialomycin D

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Use of the Mitsunobu reaction in the synthesis of polyamines

The Mitsunobu reaction has been used in the synthesis of polyamine analogues. The synthesis of the (R,R), (S,S) and meso-isomers of a tetraamine are described. The chemistry was used to synthesize a fluorinated polyamine analog and a hexaamine.