Weight | 108.184 g/mol |
---|---|
Formula | C8H12 |
Hydrogen Acceptors | 0 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 1 |
4-Vinylcyclohexene (100-40-3)
4-ethenyl-1-cyclohexene
Score:
#489 in Physics
,
#1245 in Biology
,
#1432 in Chemistry
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- TCI - 4-Vinylcyclohexene21.00 - 73.00 USD
- Involvement of apoptosis in 4-vinylcyclohexene diepoxide-induced ovotoxicity in rats. (Toxicology and Applied Pharmacology, 1996)
- The role of epoxidation in 4-vinylcyclohexene-induced ovarian toxicity. (Toxicology and Applied Pharmacology, 1990)
- Long-term effects of ovarian follicular depletion in rats by 4-vinylcyclohexene diepoxide (Reproductive Toxicology, 2002)
- Apoptosis Induced in Rats by 4-Vinylcyclohexene Diepoxide Is Associated with Activation of the Caspase Cascades (Biology of Reproduction, 2001)
- Early effects of ovotoxicity induced by 4-vinylcyclohexene diepoxide in rats and mice. (Reproductive Toxicology, 1999)
- Enhanced Expression ofbaxin Small Preantral Follicles during 4-Vinylcyclohexene Diepoxide-Induced Ovotoxicity in the Rat (Toxicology and Applied Pharmacology, 1996)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H351: Suspected of causing cancer
Warning Carcinogenicity - Category 2 - H401: Toxic to aquatic life
Hazardous to the aquatic environment, acute hazard - Category 2 - 4-ethenyl-1-cyclohexene
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SMILESC=CC1CCC=CC1
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InChIKeyBBDKZWKEPDTENS-UHFFFAOYSA-N
- Pubchem - 4-Vinylcyclohexene
- Wikipedia - 4-vinyl-1-cyclohexene
4-Vinylcyclohexene is an organic compound formed when 1,3-butadiene dimerizes in a Diels-Alder reaction. It is found in industrial processes involving 1,3-butadiene, including the manufacture of lauric acid. The 4-vinylcyclohexene formed may be sold as-is or converted to vinylcyclohexene dioxide.
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