| Weight | 112.216 g/mol |
|---|---|
| Formula | C8H16 |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 4 |
trans-2-Octene
7642-04-8, 13389-42-9, 111-67-1
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- Mammalian metabolism and environmental degradation of the juvenoid 1-(4'-ethylphenoxy)-3,7-dimethyl-6,7-epoxy-trans-2-octene and related compounds. (Journal of Agricultural and Food Chemistry, 1974)
- Multiple forms of noninduced rat liver cytochrome P-450. Metabolism of 1-(4'-ethylphenoxy)-3,7-dimethyl-6,7-epoxy-trans-2-octene by reconstituted preparations. (Journal of Biological Chemistry, 1979)
- Raman Spectra of Hydrocarbons I. 1Octene, cis+trans 2Octene, trans3Octene, trans4Octene, 4Octyne, and 1Octyne (Journal of Chemical Physics, 1943)
- Metabolic O-dealkylation of 1-(4-ethylphenoxy)-3,7-dimethyl-7-methoxy or ethoxy-trans-2-octene, potent juvenoids (Pesticide Biochemistry and Physiology, 1975)
- Relative rate constant measurements for the gas-phase reactions of hydroxyl radicals with 4-methyl-2-pentanone, trans-4-octene, and trans-2-heptene (International Journal of Chemical Kinetics, 1992)
- Thermal [2 + 2] cyclodimerisation of strained olefins. Cis, trans-1,5-cyclo-octadiene and trans-cyclo-octene (Tetrahedron, 1982)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCCCCCC=CC
-
InChIKeyILPBINAXDRFYPL-UHFFFAOYSA-N
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Synthesis
Reactant
+
1-Hydroxy-1,2-benziodoxol-3(1H)-one 1-oxide
(Nicolaou IBX dehydrogenation)
Similar Compounds
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(111-65-9, 31372-91-5, 50985-84-7)
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(2548-87-0, 2363-89-5, 25447-69-2)
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(29965-97-7, 1700-10-3)
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(57266-86-1, 2463-63-0, 18829-55-5, 29381-66-6)
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1,7-OCTADIENE
(3710-30-3)
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4-METHYL-1-PENTENE
(691-37-2, 25068-26-2)
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1,3-CYCLOHEXADIENE
(29797-09-9, 592-57-4)
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1 alternate name
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(628-81-9)
1 alternate name
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3-Methylpiperidine
(626-56-2)
1 alternate name
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trans-2-Octene
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