Chemistry:2,6-Dichloropyridine
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| Preferred IUPAC name
2,6-Dichloropyridine | |
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3D model (JSmol)
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| Properties | |
| C5H3Cl2N | |
| Molar mass | 147.99 g·mol−1 |
| Melting point | 86–89 °C (187–192 °F; 359–362 K) |
| Boiling point | 211–212 °C (412–414 °F; 484–485 K) |
| Hazards | |
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| GHS Signal word | Danger |
| H301, H315, H319, H335 | |
| P261, P264, P270, P271, P280, P301+310, P302+352, P304+340, P305+351+338, P312, P321, P330, P332+313, P337+313, P362, P403+233, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
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Tracking categories (test):
2,6-Dichloropyridine is an organohalide with the formula C5H3Cl2N. A white solid, it is one of six isomers of dichlorpyridine. It serves as a precursor to the antibiotic enoxacin.[1] 2,6-Dichoropyridine is produced by direct reaction of pyridine with chlorine. 2-Chloropyridine is an intermediate.[1]
Toxicity
The -1">50 is 115 mg/kg (oral, mice).[1]
References
- ↑ 1.0 1.1 1.2 Shimizu, Shinkichi; Watanabe, Nanao; Kataoka, Toshiaki; Shoji, Takayuki; Abe, Nobuyuki; Morishita, Sinji; Ichimura, Hisao (2007). "Ullmann's Encyclopedia of Industrial Chemistry". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a22_399.
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