| Weight | 147.992 g/mol |
|---|---|
| Formula | C5H3Cl2N |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
2,6-DICHLOROPYRIDINE (2402-78-0)
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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)
- Dichlororuthenium(IV) Complex of mesoTetrakis(2,6dichlorophenyl)porphyrin: Active and Robust Catalyst for Highly Selective Oxidation of Arenes, Unsaturated Steroids, and ElectronDeficient Alkenes by Using 2,6Dichloropyridine NOxide (Chemistry: A European Journal, 2005)
- 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)
- Adamantane Selective Hydroxylation by 2,6Dichloropyridine NOxide and Organoruthenium(II) Polyoxometalates as Catalyst Precursors (Advanced Synthesis & Catalysis, 2002)
- Orbital control in the selective photolysis of azido groups of 2,4,6-triazido-3,6-dichloropyridine (Mendeleev Communications, 2000)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC(=NC(=C1)Cl)Cl
-
InChIKeyFILKGCRCWDMBKA-UHFFFAOYSA-N
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36404-88-3
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Pyridine hydrobromide
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2-Chloro-6-methylquinoline
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3,5-DICHLOROPYRIDINE
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2,5-dichloroquinoline
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6-bromo-2-chloropyridin-3-amine
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3-bromo-2-chloro-5-methylpyridine
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6-Chloro-2,3-dimethylpyridine
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2,6-DICHLOROPYRIDINE
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