Weight | 75.498 g/mol |
---|---|
Formula | C2H2ClN |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
CHLOROACETONITRILE (107-14-2)
Score:
#486 in Physics
,
#1417 in Chemistry
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- One-step synthesis of pyrido[1,2-a]benzimidazole derivatives by a novel multicomponent reaction of chloroacetonitrile, malononitrile, aromatic aldehyde, and pyridine. (Journal of Organic Chemistry, 2009)
- Role of protonation and of axial ligands in the reductive dechlorination of alkyl chlorides by vitamin B12 complexes. Reductive cleavage of chloroacetonitrile by Co(I) cobalamins and cobinamides. (Journal of the American Chemical Society, 2005)
- A Practical Synthesis of tert-Alkylamines via the Ritter Reaction with Chloroacetonitrile (Synthesis, 2000)
- Chloroacetonitrile as eluent additive in thermospray liquid chromatography/negative ion mass spectrometry for the characterization of chlorinated organic pollutants (Journal of Mass Spectrometry, 1990)
- Chloroacetonitrile (CAN) induces glutathione depletion and 8-hydroxylation of guanine bases in rat gastric mucosa. (Journal of Biochemical and Molecular Toxicology, 1999)
- Electrochemical Synthesis of Cyanoacetic Acid from Chloroacetonitrile and Carbon Dioxide (Journal of The Electrochemical Society, 2002)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H226: Flammable liquid and vapor
Warning Flammable liquids - Category 3 - H301: Toxic if swallowed
Danger Acute toxicity, oral - Category 3 - H310: Fatal in contact with skin
Danger Acute toxicity, dermal - Category 1, 2 - H331: Toxic if inhaled
Danger Acute toxicity, inhalation - Category 3 - H401: Toxic to aquatic life
Hazardous to the aquatic environment, acute hazard - Category 2 -
SMILESC(C#N)Cl
-
InChIKeyRENMDAKOXSCIGH-UHFFFAOYSA-N
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