Weight | 117.151 g/mol |
---|---|
Formula | C8H7N |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 0 |
Aromatic Rings | 1 |
Rotatable Bonds | 1 |
Phenylacetonitrile (140-29-4)
benzyl cyanide
Score:
#2467 in Chemistry
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- Heterogeneous ethylation of phenylacetonitrile (Journal of Organic Chemistry, 1980)
- Copper-catalyzed cyanation of arenes using benzyl nitrile as a cyanide anion surrogate. (Chemical Communications, 2012)
- Synthesis of 3Cyanoindole Derivatives Mediated by Copper(I) Iodide Using Benzyl Cyanide (Journal of Organic Chemistry, 2013)
- Factors controlling the regioselectivity of additions to -enonesVI: Reactions of acetonitrile and phenylacetonitrile anions (Tetrahedron, 1978)
- Monolithium derivatives of acetonitrile and phenylacetonitrile (Journal of the American Chemical Society, 1972)
- Reactions of organic anionx. LXXIII. Alkylation of phenylacetonitrile at the interface with aqueous sodium hydroxide (Tetrahedron Letters, 1977)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H301: Toxic if swallowed
Danger Acute toxicity, oral - Category 3 - H319: Causes serious eye irritation
Warning Serious eye damage/eye irritation - Category 2A - H372: Causes damage to organs through prolonged or repeated exposure
Danger Specific target organ toxicity, repeated exposure - Category 1 - benzyl cyanide
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SMILESC1=CC=C(C=C1)CC#N
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InChIKeySUSQOBVLVYHIEX-UHFFFAOYSA-N
- Pubchem - Phenylacetonitrile
- Wikipedia - phenylacetonitrile
Benzyl cyanide (abbreviated BnCN) is an organic compound with the chemical formula C6H5CH2CN. This colorless oily aromatic liquid is an important precursor to numerous compounds in organic chemistry.
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