169302-18-5

Basic information

• Product Name: (2S,3R)-3,4-epoxy-1-phenyl-2-butanol
• Synonyms: (2S,3R)-3,4-epoxy-1-phenyl-2-butanol
• CAS NO: 169302-18-5
• Molecular Weight: 164.204
• Mol File: 169302-18-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (2S,3R)-3,4-epoxy-1-phenyl-2-butanol(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,3R)-3,4-epoxy-1-phenyl-2-butanol(169302-18-5)
• EPA Substance Registry System: (2S,3R)-3,4-epoxy-1-phenyl-2-butanol(169302-18-5)

Safety Data

• Hazardous Substances Data: 169302-18-5(Hazardous Substances Data)

Upstream product

• 122-78-1 phenylacetaldehyde 
• 6052-66-0 1-phenyl-3-buten-2-ol 

Downstream Products

• 139165-56-3 threo-(2R,3R)-1-phenyl-2,3-butanediol 
• 169302-22-1 (2R,3R)-3,4-epoxy-1-phenyl-2-butanol 
• 169057-29-8 (R)-1-(oxiran-2-yl)-2-phenylethanone 
• 169302-20-9 (2R,3R)-3,4-epoxy-1-phenyl-2-butanol 3,5-dinitrobenzoate 

Relevant articles and documents

Highly diastereo- and enantio-selective epoxidation of secondary allylic alcohols catalyzed by styrene monooxygenase

Enantiomerically enriched glycidol derivatives with contiguous stereogenic centers were obtained in a highly diastereo- and enantio-selective epoxidation catalyzed with the styrene monooxygenase StyAB2.

Synthesis of All Four Possible Stereoisomers of 1-Phenyl-2,3-butanediol and Both Enantiomers of 3-Hydroxy-4-phenyl-2-butanone to Determine the Absolute Configuration of the Natural Constituents

Enantioselective syntheses of all the possible stereoisomers of 1-phenyl-2,3-butanediol (erythro isomer 1 and threo isomer 2) and of 3-hydroxy-4-phenyl-2-butanone 3, the odor components of wisteria flowers, was accomplished via Sharpless asymmetric epoxyd