| Identification | Back Directory | [Name]
2,3,6-Trichloro-5-nitro-pyridine | [CAS]
55304-72-8 | [Synonyms]
2,5,6-Trichloro-3-nitropyridine
2,3,6-Trichloro-5-nitro-pyridine
Pyridine, 2,3,6-trichloro-5-nitro-
2,3,6-Trichloro-5-nitro-pyridine ISO 9001：2015 REACH | [Molecular Formula]
C5HCl3N2O2 | [MDL Number]
MFCD11227172 | [MOL File]
55304-72-8.mol | [Molecular Weight]
227.43 |
| Chemical Properties | Back Directory | [Melting point ]
69-71 °C | [Boiling point ]
301.1±37.0 °C(Predicted) | [density ]
1.744±0.06 g/cm3(Predicted) | [storage temp. ]
under inert gas (nitrogen or Argon) at 2-8°C | [pka]
-8.15±0.10(Predicted) | [Appearance]
Light yellow to yellow Solid |
| Hazard Information | Back Directory | [Synthesis]
General procedure for the synthesis of 2,3,6-trichloro-5-nitropyridine from 2,3,6-trichloropyridine: 2,3,6-trichloropyridine (62 mmol, 11.27 g) was dissolved in a mixture of fuming nitric acid (62 mL) and concentrated sulfuric acid (50 mL), and the reaction was heated for 12 hours at 100 °C. Upon completion of the reaction, the mixture was cooled to room temperature and carefully poured into an ice/water mixture. Subsequently, extraction was carried out with dichloromethane. The organic phases were combined, dried with anhydrous magnesium sulfate and concentrated under reduced pressure to remove the solvent to afford 2,3,6-trichloro-5-nitropyridine as a light green oil, which solidified on standing (9.65 g, 68% yield). | [References]
[1] Patent: WO2015/115673, 2015, A1. Location in patent: Page/Page column 106
[2] Patent: US2015/203450, 2015, A1. Location in patent: Paragraph 0816-0817
[3] Patent: WO2015/181747, 2015, A1. Location in patent: Page/Page column 81 |
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