| Weight | 83.134 g/mol |
|---|---|
| Formula | C5H9N |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
TRIMETHYLACETONITRILE (630-18-2)
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- Proton Magnetic Resonance Studies of Trimethylacetonitrile (Journal of Chemical Physics, 1972)
- The Reduction of Trimethylacetonitrile with Grignard Reagents1 (Journal of the American Chemical Society, 1951)
- Structure and Dynamics of Trimethylacetonitrile at the Silica/Vapor, Silica/Liquid, and Liquid/Vapor Interfaces (Journal of Physical Chemistry C, 2012)
- Notes - Reduction of Trimethylacetonitrile with Grignard Reagents. II. The Reaction of Trimethylacetonitrile with t-Butylmagnesium Chloride at Elevated Temperatures (Journal of Organic Chemistry, 1958)
- Rayleigh light scattering in molecular crystals of succinonitrile and trimethylacetonitrile (Journal of Molecular Liquids, 1984)
- ChemInform Abstract: SOLUTION EFFECT ON THE SHAPE OF THE C.TBD.N STRETCHING VIBRATION OF TRIMETHYLACETONITRILE (ChemInform, 1976)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC(C)(C)C#N
-
InChIKeyJAMNHZBIQDNHMM-UHFFFAOYSA-N
- Pubchem - TRIMETHYLACETONITRILE
- Wikipedia - Pivalonitrile
Pivalonitrile is a nitrile with the semi-structural formula (CH3)3CCN, abbreviated t-BuCN. This aliphatic organic compound is a clear, colourless liquid that is used as a solvent and as a labile ligand in coordination chemistry. Pivalonitrile is isomeric with tert-butyl isocyanide.
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(5332-06-9)
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(630-19-3)
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TRIMETHYLACETONITRILE
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