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5-CHLORO-2-METHOXYNICOTINIC ACID

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5-CHLORO-2-METHOXYNICOTINIC ACID Basic information

Product Name:
5-CHLORO-2-METHOXYNICOTINIC ACID
Synonyms:
  • 5-Chloro-2-methoxypyridine-3-carboxylic acid, 3-Carboxy-5-chloro-2-methoxypyridine
  • 5-CHLORO-2-METHOXYNICOTINIC ACID
  • 5-Chloro-2-methoxypyridine-3-carboxylic acid
  • 5-Chloro-2-methoxynicotinic acid 98%
  • 5-chloro-2-methoxy-3-pyridinecarboxylic acid
  • 3-Pyridinecarboxylic acid, 5-chloro-2-methoxy-
  • 5-Chloro-2-methoxynicotinicaci
CAS:
54916-65-3
MF:
C7H6ClNO3
MW:
187.58
Mol File:
54916-65-3.mol
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5-CHLORO-2-METHOXYNICOTINIC ACID Chemical Properties

Melting point:
146-148°
Boiling point:
301.3±37.0 °C(Predicted)
Density 
1.43
storage temp. 
Sealed in dry,Room Temperature
pka
2.99±0.10(Predicted)
form 
solid
color 
White
InChI
InChI=1S/C7H6ClNO3/c1-12-6-5(7(10)11)2-4(8)3-9-6/h2-3H,1H3,(H,10,11)
InChIKey
DPIJNAABZCWXFD-UHFFFAOYSA-N
SMILES
C1(OC)=NC=C(Cl)C=C1C(O)=O
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Safety Information

WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
2933399990
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5-CHLORO-2-METHOXYNICOTINIC ACID Usage And Synthesis

Synthesis

16498-81-0

54916-65-3

The general procedure for synthesizing 5-chloro-2-methoxynicotinic acid from 2-methoxynicotinic acid is as follows: Example 1: A. A 306 mg (0.002 mol) sample of 2-methoxynicotinic acid (product of Preparation A) was taken and added in a single addition to 20 mL of a well-stirred aqueous 5.25% sodium hypochlorite solution (Clorox). The resulting mixture (now in solution) was stirred for about 18 hours (i.e., overnight) at room temperature (about 20°C). Upon completion of the reaction, the reaction mixture was acidified with 10 mL of 1N hydrochloric acid and the resulting precipitate was subsequently extracted with chloroform. The organic extracts were combined, dried with anhydrous magnesium sulfate and filtered. The filtrate was concentrated in vacuo to give 195 mg (52% yield) of pure 5-chloro-2-methoxynicotinic acid with a melting point of 139-141 °C (melting points of 149-150 °C have been reported in the literature, based on D.E. Kuhla et al. in U.S. Patent No. 3,879,403). The pure product was further characterized by NMR data and mass spectrometry.

References

[1] Journal of Medicinal Chemistry, 1990, vol. 33, # 7, p. 1859 - 1865
[2] Synthetic Communications, 1989, vol. 19, # 9-10, p. 1505 - 1508
[3] Patent: US4980357, 1990, A
[4] Patent: US4716231, 1987, A
[5] Patent: EP306251, 1990, A3

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