| Weight | 136.238 g/mol |
|---|---|
| Formula | C10H16 |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 2 |
Alloocimene
alloocimene, (E,E)-isomer · alloocimene, (Z,Z)-isomer · alloocimene, (E,Z)-isomer
7216-56-0, 673-84-7, 3016-19-1
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- Photoisomerizations. X. Photochemical transformations of alloocimene (Journal of Organic Chemistry, 1968)
- Photochemistry of polyenes. I. Comparative study of cis-trans isomerization from the S1 and T1 states of a conjugated triene (alloocimene) (Journal of the American Chemical Society, 1971)
- Reversible triplet energy transfer between neo-alloocimene and anthracene (Chemical Physics Letters, 1984)
- Controlled/living carbocationic copolymerization of isobutylene with alloocimene (Journal of Polymer Science Part A, 2013)
- Photochemistry of polyenes. 18. Photosensitized geometric isomerization of alloocimene. The triplet torsional potential surface of a conjugated triene (The Journal of Physical Chemistry, 1981)
- Cyclopolymerization. III. Polyalloocimene (Journal of Polymer Science, 1958)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - alloocimene, (E,E)-isomer
- alloocimene, (Z,Z)-isomer
- alloocimene, (E,Z)-isomer
-
SMILESCC=C(C)C=CC=C(C)C
-
InChIKeyGQVMHMFBVWSSPF-UHFFFAOYSA-N
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Synthesis
Reactant
+
1-Hydroxy-1,2-benziodoxol-3(1H)-one 1-oxide
(Nicolaou IBX dehydrogenation)
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4-METHYL-2-PENTANOL
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Alloocimene
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