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80099-98-5

80099-98-5 Structure

80099-98-5 Structure
IdentificationBack Directory
[Name]

6-CHLORO-PYRIDINE-2-CARBONYL CHLORIDE
[CAS]

80099-98-5
[Synonyms]

6-chloropicolinoyl chloride
6-Chloropicolinic acid chloride
6-Chloro-2-pyridinecarbonyl chloride
6-CHLORO-PYRIDINE-2-CARBONYL CHLORIDE
2-Pyridinecarbonylchloride, 6-chloro-
2-Pyridinecarbonyl chloride, 6-chloro- (9CI)
6-CHLORO-PYRIDINE-2-CARBONYL CHLORIDE ISO 9001:2015 REACH
[Molecular Formula]

C6H3Cl2NO
[MDL Number]

MFCD00274531
[MOL File]

80099-98-5.mol
[Molecular Weight]

176
Chemical PropertiesBack Directory
[Boiling point ]

239.0±20.0 °C(Predicted)
[density ]

1.454±0.06 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[pka]

-2.22±0.10(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]

GHS hazard pictograms
GHS05
[Signal word ]

Danger
[Hazard statements ]

H314
[Precautionary statements ]

P260-P280
[HS Code ]

2933399990
Hazard InformationBack Directory
[Synthesis]

6-Hydroxypicolinic acid

19621-92-2

6-CHLORO-PYRIDINE-2-CARBONYL CHLORIDE

80099-98-5

General procedure for the synthesis of 6-chloropyridinecarbonyl chloride from 6-hydroxypyridine-2-carboxylic acid: to 20 g (144 mmol) of 6-hydroxypyridine-2-carboxylic acid was added 50.6 g (330 mmol) of phosphorus trichloride and 99.8 g (479 mmol) of phosphorus pentachloride, and the reaction was carried out by stirring the mixture for 8 hours at 90 °C. Upon completion of the reaction, the mixture was cooled, followed by the addition of 8.6 g of formic acid, and the reaction mixture was concentrated using a rotary evaporator to quantitatively obtain the target product 6-chloropyridinecarbonyl chloride.

[References]

[1] Patent: US2004/14977, 2004, A1. Location in patent: Page 20
[2] Patent: EP1302466, 2003, A1
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