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2-Chloro-6-methoxyisonicotinic acid

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2-Chloro-6-methoxyisonicotinic acid Basic information

Product Name:
2-Chloro-6-methoxyisonicotinic acid
Synonyms:
  • 2-Chloro-6-methoxypyridine-4-carboxylic acid, 4-Carboxy-2-chloro-6-methoxypyridine
  • 2-Chloro-6-methoxy-4-pyridinecarboxylic acid
  • 2-Chloro-6-methoxypyridine-4-c
  • TIMTEC-BB SBB005427
  • 2-CHLORO-6-METHOXYISONICOTINIC ACID
  • 2-CHLORO-6-METHOXYPYRIDINE-4-CARBOXYLIC ACID
  • BUTTPARK 43\57-34
  • 4-Pyridinecarboxylic acid, 2-chloro-6-methoxy-
CAS:
15855-06-8
MF:
C7H6ClNO3
MW:
187.58
Product Categories:
  • Carboxylic Acids
  • Pyridines
  • Carboxylic Acids
Mol File:
15855-06-8.mol
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2-Chloro-6-methoxyisonicotinic acid Chemical Properties

Melting point:
214 °C
Boiling point:
209-213℃
Density 
1.430±0.06 g/cm3(Predicted)
storage temp. 
Store at room temperature
form 
powder
pka
2.88±0.10(Predicted)
color 
White
InChIKey
PJQBTHQTVJMCFX-UHFFFAOYSA-N
CAS DataBase Reference
15855-06-8(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36/37/39-37/39-36/37
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
2933399990
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2-Chloro-6-methoxyisonicotinic acid Usage And Synthesis

Synthesis

67-56-1

5398-44-7

15855-06-8

a) 2,6-Dichloroisonicotinic acid (200 g, 1.04 mol) was dissolved in methanol (3 L) and 32% aqueous sodium hydroxide solution (770 mL) was added. The stirred mixture was heated to 34°C, then warmed to 70°C and kept at this temperature for 4 hours of reaction. After the reaction was completed, it was cooled to room temperature. The reaction mixture was neutralized with 32% aqueous hydrochloric acid solution (100 mL) and 25% aqueous hydrochloric acid solution (700 mL). The mixture was stirred at room temperature overnight. The white precipitate formed was collected by filtration, washed with methanol and dried. The filtrate was evaporated and the residue was suspended in water (200 mL). The resulting mixture was heated to 60 °C and the solid product was collected, washed with water and dried. All products were combined to give 2-chloro-6-methoxyisonicotinic acid (183 g) as a white solid; LC-MS: t R = 0.80 min, [M + 1] + = 187.93.

References

[1] Tetrahedron, 2002, vol. 58, # 34, p. 6951 - 6963
[2] Organic Letters, 2000, vol. 2, # 22, p. 3421 - 3423
[3] Patent: WO2011/7324, 2011, A1. Location in patent: Page/Page column 20
[4] Patent: US2012/108638, 2012, A1. Location in patent: Page/Page column 8
[5] Patent: US2013/303514, 2013, A1. Location in patent: Paragraph 0192

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