Weight | 86.178 g/mol |
---|---|
Formula | C6H14 |
Hydrogen Acceptors | 0 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
2,2-DIMETHYLBUTANE
75-83-2, 79-29-8, 107-83-5, 96-14-0
Score:
#614 in Physics
,
#1784 in Chemistry
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- Solvent Effects in the Reactions of Free Radicals and Atoms. II. Effects of Solvents on the Position of Attack of Chlorine Atoms upon 2,3-Dimethylbutane, Isobutane and 2-Deuterio-2-methylpropane1 (Journal of the American Chemical Society, 1958)
- Rotational isomerism. XI. Raman spectra of nbutane, 2methylbutane, and 2, 3dimethylbutane (Journal of Chemical Physics, 1974)
- Dielectric Relaxations in Various Crystal Modifications of Cyclohexanol and 2,3-Dimethylbutane (Molecular Crystals and Liquid Crystals, 1972)
- Kinetic study of the photochlorination of 2,3-dimethylbutane and other alkanes in solution in the presence of benzene. First measurements of the absolute rate constants for hydrogen abstraction by the "free" chlorine atom and the chlorine atom-benzene .pi.-complex. Identification of these two species as the only hydrogen abstractors in these systems (Journal of the American Chemical Society, 1985)
- Calorimetric Study of the Glassy State. VI. Phase Changes in Crystalline and Glassy-Crystalline 2,3-Dimethylbutane (Bulletin of the Chemical Society of Japan, 1971)
- Structure H and Structure I Hydrate Equilibrium Data for 2,2-Dimethylbutane with Methane and Xenon (Journal of Chemical & Engineering Data, 1996)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H225: Highly Flammable liquid and vapor
Danger Flammable liquids - Category 2 - H315: Causes skin irritation
Warning Skin corrosion/irritation - Category 2 - H411: Toxic to aquatic life with long lasting effects
Hazardous to the aquatic environment, long-term hazard - Category 2 -
SMILESCCC(C)(C)C
-
InChIKeyHNRMPXKDFBEGFZ-UHFFFAOYSA-N
- Pubchem - 2,2-DIMETHYLBUTANE
- Wikipedia - 2,2-dimethylbutane
2,2-Dimethylbutane, trivially known as neohexane, is an organic compound with formula C6H14 or (H3C-)3-C-CH2-CH3. It is therefore an alkane, indeed the most compact and branched of the hexane isomers the only one with a quaternary carbon and a butane (C4) backbone. It can be synthesised by the hydroisomerisation of 2,3-dimethylbutane using an acid catalyst.
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