| Weight | 80.13 g/mol |
|---|---|
| Formula | C6H8 |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
1,4-CYCLOHEXADIENE (628-41-1)
cyclohexadiene
Score:
#2309 in Physics
,
#7113 in Chemistry
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- Sigma-Aldrich - 1,4-CYCLOHEXADIENE36.80 - 372.00 USD
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- TCI - 1,4-CYCLOHEXADIENE111.00 - 224.00 USD
- Rapid removal of protecting groups from peptides by catalytic transfer hydrogenation with 1,4-cyclohexadiene (Journal of Organic Chemistry, 1978)
- Metabolism of benzoic acid by bacteria. Accumulation of (-)-3,5-cyclohexadiene-1,2-diol-1-carboxylic acid by a mutant strain of Alcaligenes eutrophus (Biochemistry, 1971)
- Galvinoxyl (2,6-Di-tert-butyl--(3,5-di-tert-butyl-4-oxo-2,5-cyclohexadiene-1-ylidene)-p-tolyloxy) as a Scavenger of Shorter-lived Free Radicals (Journal of the American Chemical Society, 1962)
- Time-resolved dissociative intense-laser field ionization for probing dynamics: Femtosecond photochemical ring opening of 1,3-cyclohexadiene (Journal of Chemical Physics, 2000)
- Thermal and Photosensitized Dimerizations of Cyclohexadiene (Journal of the American Chemical Society, 1964)
- Structure et synthse de la damascnone (trimthyl-2,6,6-trans-crotonoyl-1-cyclohexadine-1,3), constituant odorant de l'essence de rose bulgare (rosa damascena Mill. (Helvetica Chimica Acta, 1970)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - cyclohexadiene
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SMILESC1C=CCC=C1
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InChIKeyUVJHQYIOXKWHFD-UHFFFAOYSA-N
- Pubchem - 1,4-CYCLOHEXADIENE
- Wikipedia - 1,4-cyclohexadiene
1,4-Cyclohexadiene is an organic compound with the formula C6H8. It is a colourless, flammable liquid that is of academic interest as a prototype of a large class of related compounds called terpenoids, an examples being -terpinene. An isomer exists of this compound, 1,3-cyclohexadiene.
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1,4-CYCLOHEXADIENE
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