Weight | 147.992 g/mol |
---|---|
Formula | C5H3Cl2N |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 0 |
Aromatic Rings | 1 |
Rotatable Bonds | 0 |
2,4-DICHLOROPYRIDINE (26452-80-2)
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- Analysis of vibrational spectra of 4-amino-2,6-dichloropyridine and 2-chloro-3,5-dinitropyridine based on density functional theory calculations (Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2006)
- LACK OF DNA BINDING IN THE RAT NASAL MUCOSA AND OTHER TISSUES OF THE NASAL TOXICANTS ROFLUMILAST, A PHOSPHODIESTERASE 4 INHIBITOR, AND A METABOLITE, 4-AMINO-3,5-DICHLOROPYRIDINE, IN CONTRAST TO THE NASAL CARCINOGEN 2,6-DIMETHYLANILINE* (Drug and Chemical Toxicology, 2002)
- Synthesis and regioselective cycloaddition reactions of 2,4,6-triazido-3,5-dichloropyridine (Mendeleev Communications, 1999)
- Orbital control in the selective photolysis of azido groups of 2,4,6-triazido-3,6-dichloropyridine (Mendeleev Communications, 2000)
- Photoassisted oxygenation of alkane catalyzed by ruthenium complexes using 2,6-dichloropyridine N-oxide under visible light irradiationElectronic supplementary information (ESI) available: syntheses of the complexes, crystallographic data of complex 4 (Table S-1), 1H NMR spectra before and after irradiation (Fig. S-1, S-2, S-3, S-5), UV-vis spectral change (Fig. S-4, S-6). See http://www.rsc.org/suppdata/cc/b3/b316970g/ (Chemical Communications, 2004)
- Regioselective Addition of Mesitol to a 2,4-Dichloropyridine (Organic Process Research & Development, 2008)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CN=C(C=C1Cl)Cl
-
InChIKeyTYPVHTOETJVYIV-UHFFFAOYSA-N
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