Weight | 144.388 g/mol |
---|---|
Formula | C2Cl3N |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
TRICHLOROACETONITRILE (545-06-2)
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- Epoxidation of alkenes with trichloroacetonitrile/hydrogen peroxide in a neutral biphasic solvent system (Journal of Organic Chemistry, 1983)
- Teratogenic effects of trichloroacetonitrile in the longevans rat (Teratology, 1988)
- Catalytic Asymmetric Oxidation of N-Sulfonyl Imines with Hydrogen PeroxideTrichloroacetonitrile System (Journal of the American Chemical Society, 2013)
- Studies on s-Triazines. I. Cotrimerization of Trichloroacetonitrile with Other Nitriles (Bulletin of the Chemical Society of Japan, 1969)
- A CONVENIENT METHOD FOR SYNTHESIS OF SYMMETRICAL ACID ANHYDRIDES FROM CARBOXYLIC ACIDS WITH TRICHLOROACETONITRILE AND TRIPHENYLPHOSPHINE (Synthetic Communications, 2001)
- Metal-catalyzed reactions of -dicarbonyls with trichloroacetonitrile: synthesis of -trichloromethylenaminodiones (Journal of Molecular Catalysis, 1986)
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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 - H302: Harmful if swallowed
Warning Acute toxicity, oral - Category 4 - H315: Causes skin irritation
Warning Skin corrosion/irritation - Category 2 - H331: Toxic if inhaled
Danger Acute toxicity, inhalation - Category 3 - H410: Very toxic to aquatic life with long lasting effects
Warning Hazardous to the aquatic environment, long-term hazard - Category 1 -
SMILESC(#N)C(Cl)(Cl)Cl
-
InChIKeyDRUIESSIVFYOMK-UHFFFAOYSA-N
- Pubchem - TRICHLOROACETONITRILE
- Wikipedia - Trichloroacetonitrile
Trichloroacetonitrile is an organic compound with the formula CCl3CN. It is a colourless liquid, although commercial samples often are brownish. It is used commercially as a precursor to the fungicide etridiazole.
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