| Weight | 84.162 g/mol |
|---|---|
| Formula | C6H12 |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 2 |
2-METHYL-1-PENTENE (27236-46-0, 763-29-1)
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- Sigma-Aldrich - 2-METHYL-1-PENTENE44.70 - 148.00 USD
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- A Cyclometalated Aryloxy(chloro)neopentylidenetungsten Complex: A Highly Active and Stereoselective Catalyst for the Metathesis of cis and trans2Pentene, Norbornene, 1Methylnorbornene, and Ethyl Oleate (Angewandte Chemie, 1992)
- Addition reactions of diarylcarbenium ions to 2-methyl-1-pentene. kinetic method and reaction mechanism (Journal of the American Chemical Society, 1990)
- Efficient Incorporation of 2-Methyl-1-pentene in Copolymerization of Ethylene with 2-Methyl-1-pentene Catalyzed by Nonbridged Half-Titanocenes (Macromolecules, 2005)
- Anionic Activation of C-H Bonds in Olefins. III. Solvent Effect on the Isomerization of 2-Methyl-1-pentene (Journal of the American Chemical Society, 1962)
- Effect of cyclopentadienyl and anionic donor ligands on monomer reactivities in copolymerization of ethylene with 2-methyl-1-pentene by nonbridged half-titanocenes-cocatalyst systems (Macromolecules, 2007)
- Stereochemistry of the iodocarbonatation of cis- and trans-3-methyl-4-pentene-1,2-diols: the unusual formation of several anti iodo carbonates (Journal of Organic Chemistry, 1993)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCCCC(=C)C
-
InChIKeyWWUVJRULCWHUSA-UHFFFAOYSA-N
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Reactant
+
1-Hydroxy-1,2-benziodoxol-3(1H)-one 1-oxide
(Nicolaou IBX dehydrogenation)
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2-METHYL-1-PENTENE
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