| Weight | 110.2 g/mol |
|---|---|
| Formula | C8H14 |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 4 |
1,3-Octadiene
39491-65-1, 63597-41-1, 1002-33-1
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- Dialkylation of 2,3-butanedione diketal with 1,8-bis(trimethylsilyl)-2,6-octadiene (BISTRO). Application to the synthesis of estrone derivatives (Tetrahedron, 1996)
- Acylation of 1,3-bis(trimethylsilyl)-propene and 1,8-bis(trimethylsliyl)-1,7-octadiene. Obtention of ()-1-alkyl-2,5-divinylcyclopentanols. (Tetrahedron, 1988)
- Palladium(0)catalysed conversion of acetylenic epoxides into allenic alcohols. Novel route to ()2,3octadiene5,7diyn1ol, a metabolite from fungus Cortinellus berkeleyanus (Recueil des Travaux Chimiques des Pays-Bas, 2010)
- (3R,4S,7S)-trans, trans-3,7-Dimethyl-1,8,8-tribromo-3,4,7-trichloro-1,5-octadiene, a novel monoterpene from the sea hare, Aplysia californica (Journal of the American Chemical Society, 1973)
- Wagner-Meerwein rearrangements in the solvolyses of benzobicyclo[2.2.2]octenyl and -octadienyl brosylates and nuclear magnetic resonance spectra of the benzobicyclo[3.2.1]octadiene and benzo[3,4]tricyclo[3.2.1.02,7]octene systems (Journal of the American Chemical Society, 1967)
- Catalysis by palladium salts IV. Selective hydrogenation with formic acid in the palladium catalysed dimerisation of 1,3-butadiene; Syntheses of 1,7-octadiene (Journal of Organometallic Chemistry, 1973)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCCCCC=CC=C
-
InChIKeyQTYUSOHYEPOHLV-UHFFFAOYSA-N
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Synthesis
4,4-Dimethyl-5-decene-2-one
+
1-Hydroxy-1,2-benziodoxol-3(1H)-one 1-oxide
(Nicolaou IBX dehydrogenation)
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