1-acetyl-1-cyclohexene

1-(cyclohexen-1-yl)ethanone

CAS: 932-66-1 C8 H12 O MW: 124.18284000

Identification

Name1-acetyl-1-cyclohexene
IUPAC1-(cyclohexen-1-yl)ethanone
CAS Number932-66-1
EINECS213-256-5
FDA UNII7539U6WQBL
Molecular FormulaC8 H12 O
Molecular Weight124.18284000
MDL NumberMFCD00001547
Nikkaji NumberJ80.022H

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Specific Gravity 0.96600 @ 25.00 °C.
Refractive Index 1.49000 @ 20.00 °C.
Melting Point 73.00 °C. @ 760.00 mm Hg
Boiling Point 201.50 °C. @ 760.00 mm Hg
Vapor Pressure 0.304000 mmHg @ 25.00 °C. (est)
Flash Point 150.00 °F. TCC ( 65.56 °C. )
logP (o/w) 1.648 (est)
Soluble in water, 1188 mg/L @ 25 °C (est)

No sensory data available

Safety Information

Preferred SDSView
Oral/Parenteral ToxicityNot determined
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Categorynatural substances and extractives
Recommendation for 1-acetyl-1-cyclohexene usage levels up tonot for fragrance use.
Recommendation for 1-acetyl-1-cyclohexene flavor usage levels up tonot for flavor use.

BOC Sciences

Best of Chemicals Supplier

Quality supplier of research chemicals and biochemicals including inhibitors, building blocks, GMP Products, impurities and metabolites, APIs for Veterinary, Natural Compounds, ADCs, Stem Cell Molecul...

View All Website 1-631-485-4226 account@bocsci.com

Potential Uses

None Found

Natural Occurrence

not found in nature

Synonyms

1- acetylcyclohex-1-ene 1- acetylcyclohexene 1-( cyclohex-1-en-1-yl)ethanone 1- cyclohex-1-en-1-ylethanone 1- cyclohex-1-enyl ethanone cyclohex-1-enyl methyl ketone cyclohex-1-enylmethylketone 1- cyclohexen-1-yl methyl ketone 1-( cyclohexen-1-yl)ethanone 1-(1- cyclohexen-1-yl)ethanone cyclohexene, 1-acetyl- ethanone, 1-(1-cyclohexen-1-yl)- ketone, cyclohex-1-enyl methyl methyl 1-cyclohexenyl ketone PubMed: Chemoenzymatic Synthesis of Enantiomeric, Bicyclic d-Halo-gamma-lactones with a Cyclohexane Ring, Their Biological Activity and Interaction with Biological Membranes