77931-76-1

Basic information

• Product Name: 2-tert-butylcyclohex-2-en-1-ol
• Synonyms: 2-tert-butylcyclohex-2-en-1-ol
• CAS NO: 77931-76-1
• Molecular Weight: 154.252
• Mol File: 77931-76-1.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 2-tert-butylcyclohex-2-en-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-tert-butylcyclohex-2-en-1-ol(77931-76-1)
• EPA Substance Registry System: 2-tert-butylcyclohex-2-en-1-ol(77931-76-1)

Safety Data

• Hazardous Substances Data: 77931-76-1(Hazardous Substances Data)

Upstream product

• 107932-21-8 2-t-butyl-2-cyclohexen-1-one 
• 3419-66-7 1-tert-butyl-1-cyclohexene 
• 253185-03-4 tert-butylbenzene 
• 107932-20-7 2-t.butyl-2-chlorocyclohexanone 
• 1728-46-7 2-tert-butylcyclohexanone 
• 7583-74-6 1,2-epoxy-1-t-butylcyclohexane 
• 147544-32-9 2-tert-Butyl-cyclohex-2-enyl-hydroperoxide 

Downstream Products

• 107932-19-4 all-cis-2-t.butyl-1,3-cyclohexanediol 
• 107932-18-3 all-trans-2-t.butyl-1,3-cyclohexanediol 
• 37435-26-0 2-t.butyl-1,3-cyclohexanedione 
• 107932-17-2 cis,trans-2-t.butyl-1,3-cyclohexanediol 

Relevant articles and documents

Novel Catalytic Kinetic Resolution of Racemic Epoxides to Allylic Alcohols

(Matrix Presented) The kinetic resolution of racemic epoxides via catalytic enantioselective rearrangement to allylic alcohols was investigated. Using the Li-salt of (1S,3R,4R)-3-(pyrrolidinyl)methyl-2-azabicyclo [2.2.1] heptane 1 as catalyst allowed both

Regioselective formation of cyclic and allylic hydroperoxides

A regioselective photosensitized oxygenation is reported for the preparation of cyclic and allylic hydroperoxides.

ON THE SYNTHESIS AND CONFORMATIONAL ASPECTS OF 2-METHYL AND 2-t.BUTYL SUBSTITUTED 1,3-CYCLOPENTANE AND CYCLOHEXANE DIOLS

The diastereomers of 2-methyl-1,3-cyclopentanediol, 2-t.butyl-1,3-cyclopentanediol, 2-methyl-1,3-cyclohexanediol and 2-t.butyl-1,3-cyclohexanediol have been prepared.Configurational assignment and some conformational aspects are described.