Weight | 147.992 g/mol |
---|---|
Formula | C5H3Cl2N |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 0 |
Aromatic Rings | 1 |
Rotatable Bonds | 0 |
2,3-DICHLOROPYRIDINE (2402-77-9)
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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)
- Synthesis of tetraarylpyridines by chemo-selective Suzuki-Miyaura reactions of 3,5-dibromo-2,6-dichloropyridine. (Organic and Biomolecular Chemistry, 2015)
- The remote-oxyfunctionalization of unactivated carbons in (5)-3-oxobile acids by 2,6-dichloropyridine N-oxide catalyzed by rutheniumporphyrin and HBr: a direct lactonization at C-20 (Organic and Biomolecular Chemistry, 2004)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC(=C(N=C1)Cl)Cl
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InChIKeyMAKFMOSBBNKPMS-UHFFFAOYSA-N
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Similar Compounds
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4-Amino-3-chloropyridine
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5-Amino-2-chloropyridine
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2402-95-1
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5-Chloropyridin-3-ol
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1,7-dichloroisoquinoline
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2-Chloro-4-nitropyridine
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2-Chloro-3-cyanopyridine
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4-CHLOROPYRIDINE
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4-Chloropyridine hydrochloride
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2-chloropyridine-3,4-diamine
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2-Chloro-3-ethylpyridine
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2,4-Dichloro-1,5-naphthyridine
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N-(2-chloropyridin-4-yl)acetamide
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1-(2-chloro-4-pyridinyl)ethanone
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1-(6-chloro-3-pyridinyl)-N,N-dimethylmethanamine
(221146-31-2)
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2,6-Dichloro-4-(trichloromethyl)pyridine
(22652-14-8)
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