7360-39-6

Basic information

• Product Name: 4-tert-butylcyclohex-1-en-1-yl acetate
• CAS NO: 7360-39-6
• Molecular Formula: C₁₂H₂₀O₂
• Molecular Weight: 196.286
• Mol File: 7360-39-6.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 267.5°C at 760 mmHg
• Flash Point: 106.2°C
• Density: 0.95g/cm³
• Vapor Pressure: 0.00814mmHg at 25°C
• Refractive Index: 1.467
• CAS DataBase Reference: 4-tert-butylcyclohex-1-en-1-yl acetate(CAS DataBase Reference)
• NIST Chemistry Reference: 4-tert-butylcyclohex-1-en-1-yl acetate(7360-39-6)
• EPA Substance Registry System: 4-tert-butylcyclohex-1-en-1-yl acetate(7360-39-6)

Safety Data

• Hazardous Substances Data: 7360-39-6(Hazardous Substances Data)

Upstream product

• 98-53-3 4-tercbutyl-cyclohexanone 
• 64-19-7 acetic acid 
• 10534-59-5 tetrabutylammonium acetate 
• 19980-19-9 4-t-butyl-1-trimethylsilyloxy-1-cyclohexene 
• 75-36-5 acetyl chloride 
• 108-22-5 Isopropenyl acetate 
• 108-24-7 acetic anhydride 

Downstream Products

• 128298-81-7 2-hydroxy-4-t-butylcyclohexanone 
• 86023-58-7 cis/trans-2-Acetoxy-4-tert-butylcyclohexanone 
• 69217-91-0 2,7-Di-tert-butyl-octahydro-dibenzo[1,4]dioxine-4a,9a-diol 
• 132091-74-8 4-(tert-butyl)-2-(trifluoromethyl)cyclohexan-1-one 
• 5064-52-8 2-methyl-4-tert-butylcyclohexanone 
• 43131-76-6 (C₄H₉)3SnO(C₆H₈C₄H₉) 
• 73977-82-9 Benzoic acid 5-tert-butyl-2-fluoro-cyclohept-2-enyl ester 
• 5581-94-2 3-tert-Butyl-cyclopentanone 
• 77299-79-7 trans 2-α-iodo-4-t-butyl-cyclohexanone 
• 3211-27-6 4-tert-butyl-2-methylcyclohexanone 
• 15649-48-6 1-Acetoxy-2-aethyl-4-tert.-butyl-cyclohexen-⁽¹⁾ 
• 3393-97-3 1-ethoxy-4-tert-butylcyclohexene 
• 74609-74-8 trans-2-nitro-4-tert-butylcyclohexanone 
• 74609-73-7 cis-2-nitro-4-tert-butylcyclohexanone 

Relevant articles and documents

Reductive Coupling between C-N and C-O Electrophiles

The cross-electrophile reaction is a promising strategy for C-C bond formation. Recent studies have focused mainly on reactions with organic halides. Here we report a coupling reaction between C-N and C-O electrophiles that demonstrates the possibility of constructing a C-C bond via C-N and C-O cleavage. Several reactions between benzyl/aryl ammonium salts and vinyl/aryl C-O electrophiles have been studied. Preliminary mechanistic studies revealed that the benzyl ammoniums were activated through a radical mechanism.

Cyclohexynes. Generation from iodonium salts and regioselective reaction with nucleophile

Cyclohexynes are effectively generated by treatment of cyclohex-1-enyliodonium salts with a mild base such as acetate and fluoride ion in chloroform. Regioselectivity of the nucleophilic addition of acetate ion to cyclohexynes depends on the 4-substituent