53921-01-0

Basic information

• Product Name: trans-Bromo-4-hydroxy-3-cyclohexen
• Synonyms: trans-Bromo-4-hydroxy-3-cyclohexen
• CAS NO: 53921-01-0
• Molecular Weight: 177.041
• Mol File: 53921-01-0.mol

Chemical Properties

• CAS DataBase Reference: trans-Bromo-4-hydroxy-3-cyclohexen(CAS DataBase Reference)
• NIST Chemistry Reference: trans-Bromo-4-hydroxy-3-cyclohexen(53921-01-0)
• EPA Substance Registry System: trans-Bromo-4-hydroxy-3-cyclohexen(53921-01-0)

Safety Data

• Hazardous Substances Data: 53921-01-0(Hazardous Substances Data)

Upstream product

• 1165952-91-9 cyclohexa-1,3-diene 

Downstream Products

• 129217-16-9 (3aR,7aS)-3-Benzoyl-3a,4,5,7a-tetrahydro-3H-benzooxazol-2-one 
• 129217-15-8 (1R*)-6(R*)-bromocyclohex-2-enyl benzoylcarbamate 

Relevant articles and documents

Dramatic behavioral differences of the copolymerization reactions of 1,4-cyclohexadiene and 1,3-cyclohexadiene oxides with carbon dioxide

The copolymerization of 1,3-cyclohexadiene oxide (1,2-epoxy-3-cyclohexene) with CO2 in the presence of the binary catalyst (salen)CoX or (salen)CrX and onium salts was shown to selectively afford the completely alternating copolymer poly(1,3-cy

N-BENZOYLCARBAMATE CYCLIZATIONS

The anion of an alcohol derived N-benzoylcarbamate may be used to deliver nitrogen intramolecularly to electrophilic centers.This allows the stereocontrolled synthesis of a variety of amino-alcohol and amino-diol derivatives.