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6-Chloro-pyridine-2-carbonyl chloride

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6-Chloro-pyridine-2-carbonyl chloride manufacturers

6-Chloro-pyridine-2-carbonyl chloride Basic information
Product Name:6-Chloro-pyridine-2-carbonyl chloride
Synonyms:2-Pyridinecarbonyl chloride, 6-chloro- (9CI);6-Chloro-2-pyridinecarbonyl chloride;6-Chloropicolinic acid chloride;2-Pyridinecarbonylchloride, 6-chloro-;6-CHLORO-PYRIDINE-2-CARBONYL CHLORIDE ISO 9001:2015 REACH;2-Chloro-6-pyridylcarbonyl chloride;6-chloropicolinoyl chloride;6-Chloro-pyridine-2-carbonyl chloride
CAS:80099-98-5
MF:C6H3Cl2NO
MW:176
EINECS:
Product Categories:ACIDHALIDE
Mol File:80099-98-5.mol
6-Chloro-pyridine-2-carbonyl chloride Structure
6-Chloro-pyridine-2-carbonyl chloride Chemical Properties
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 Information
HS Code 2933399990
MSDS Information
6-Chloro-pyridine-2-carbonyl chloride Usage And Synthesis
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
6-Chloro-pyridine-2-carbonyl chloride Preparation Products And Raw materials
Raw materials6-Hydroxypicolinic acid
Tag:6-Chloro-pyridine-2-carbonyl chloride(80099-98-5) Related Product Information
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