| Weight | 80.13 g/mol |
|---|---|
| Formula | C6H8 |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
Methylcyclopentadiene
26519-91-5, 96-39-9, 26472-00-4
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- SolventFree Conversion of Linalool to Methylcyclopentadiene Dimers: A Route To Renewable HighDensity Fuels (Chemsuschem, 2011)
- The pyrolysis of methylcyclopentadiene: Isomerization and formation of aromatics (2000)
- The crystal and molecular structure of dimethyl--cyclopentadienyl(methylcyclopentadiene)rhenium (Journal of The Chemical Society A: Inorganic, Physical, Theoretical, 1967)
- Regioselectivity of Lewis acid catalyzed Diels-Alder reactions of methylcyclopentadiene (Journal of Organic Chemistry, 1975)
- Decomposition and ring expansion in methylcyclopentadiene: single-pulse shock tube and modeling study (2005)
- A [1,5] sigmatropic hydrogen shift induced by high vibrational overtone excitation: the isomerization of 2-methylcyclopentadiene (The Journal of Physical Chemistry, 1983)
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- Pubchem - Methylcyclopentadiene
- Wikipedia - Methylcyclopentadiene
Methylcyclopentadiene is any of three isomeric cyclic dialkenes with the formula C5MeH5 (Me = CH3). These isomers are the organic precursor to the methylcyclopentadienyl ligand (C5H4Me, often denoted as Cp), commonly found in organometallic chemistry. As with cyclopentadiene, methylcyclopentadiene is prepared by thermal cracking of its DielsAlder dimer, followed by distillation for removal of cyclopentadiene, a common impurity.
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