| Weight | 138.557 g/mol |
|---|---|
| Formula | C6H3ClN2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
2-Chloro-3-cyanopyridine (6602-54-6)
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- Characterization of a newly isolated strain Rhodococcus erythropolis ZJB-09149 transforming 2-chloro-3-cyanopyridine to 2-chloronicotinic acid (New Biotechnology, 2011)
- Synthesis of 2-chloro-5-hydroxynicotinonitrile: The required intermediate in the total synthesis of a hydroxylated metabolite of (S)-2-(3-t-butylamino-2-hydroxypropoxy)-3-cyanopyridine (Journal of Heterocyclic Chemistry, 1980)
- Nucleophilic replacement of the azido groups by amines in 2,4,6-triazido-3-chloro-5-cyanopyridine (Mendeleev Communications, 2007)
- Synthesis and regioselective cycloaddition reaction of 2,4,6-triazido-3-chloro-5-cyanopyridine with norbornene (Chemistry of Heterocyclic Compounds, 1993)
- 1,3-Dipolar tris-cycloaddition oftert-butylphosphaacetylene to 2,4,6-triazido-3-chloro-5-cyanopyridine (Russian Chemical Bulletin, 1996)
- 3-Cyanopyridine-2-chloro-4-nitrobenzoic acid (1/1) (Acta Crystallographica Section E-structure Reports Online, 2004)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC(=C(N=C1)Cl)C#N
-
InChIKeyJAUPUQRPBNDMDT-UHFFFAOYSA-N
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