| Weight | 87.509 g/mol |
|---|---|
| Formula | C3H2ClN |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
2-Chloroacrylonitrile (920-37-6)
alpha-chloroacrylonitrile
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- Asymmetric Conjugate Addition of Oxindoles to 2-Chloroacrylonitrile: A Highly Effective Organocatalytic Strategy for Simultaneous Construction of 1,3-Nonadjacent Stereocenters Leading to Chiral Pyrroloindolines (Chemistry: A European Journal, 2010)
- 2-Chloroacrylonitrile as a cyclodipolarophile in 1,3-cycloadditions. 3-Cyanopyrroles (Journal of Organic Chemistry, 1978)
- Novel reaction of o-phenolic Mannich bases with .alpha.-chloroacrylonitrile (Journal of Organic Chemistry, 1980)
- Base-catalyzed reaction of hydrogen sulfide with methyl .alpha.-chloroacrylate and .alpha.-chloroacrylonitrile (Journal of Organic Chemistry, 1969)
- Genotoxicity of 2-halosubstituted enals and 2-chloroacrylonitrile in the Ames test and the SOS-chromotest (Mutation Research\/genetic Toxicology, 1994)
- Characterization of the 2-Chloroacrylonitrile Negative Ion Using Photoelectron and Photofragmentation Spectroscopies (The Journal of Physical Chemistry, 1995)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - alpha-chloroacrylonitrile
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SMILESC=C(C#N)Cl
-
InChIKeyOYUNTGBISCIYPW-UHFFFAOYSA-N
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