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5-METHOXYPYRIDINE-2-CARBOXYLIC ACID

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5-METHOXYPYRIDINE-2-CARBOXYLIC ACID Basic information

Product Name:
5-METHOXYPYRIDINE-2-CARBOXYLIC ACID
Synonyms:
  • 5-METHOXYPICOLINIC ACID
  • 5-METHOXYPYRIDINE-2-CARBOXYLIC ACID
  • 5-METHOXY-2-PYRIDINECARBOXYLIC ACID
  • 5-METHOXYPYRIDINE-2-CARBOXYLIC ACID, 98+%
  • 5-METHOXYPYRIDINE-2-CARBOXLIC ACID
  • 5-Methoxypyridine-2-carboxylic acid 5-Methoxy-2-pyridinecarboxylic acid
  • 5-Methoxy-2-pyridinecarboxylic acid, 95+%
  • 5-Methoxy-2-pyridinecarboxyL
CAS:
29082-92-6
MF:
C7H7NO3
MW:
153.14
EINECS:
1533716-785-6
Product Categories:
  • Pyridines
  • Heterocycle-Pyridine series
  • Amino Acids & Derivatives
  • Aromatics
Mol File:
29082-92-6.mol
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5-METHOXYPYRIDINE-2-CARBOXYLIC ACID Chemical Properties

Melting point:
172-174 °C
Boiling point:
312.9±22.0 °C(Predicted)
Density 
1.284±0.06 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Room Temperature
pka
1.07±0.50(Predicted)
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Safety Information

HS Code 
2933399990
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5-METHOXYPYRIDINE-2-CARBOXYLIC ACID Usage And Synthesis

Uses

A natural imino acid.

Synthesis

29681-39-8

29082-92-6

B) Synthesis of 5-methoxypyridine-2-carboxylic acid: a solution of lithium hydroxide monohydrate (5.0 g) in water (10 mL) was added to a solution of methyl 5-methoxypyridine-2-carboxylate (4.0 g) in methanol (50 mL) at room temperature. The reaction mixture was stirred at room temperature for 12 hours. Subsequently, the pH of the reaction mixture was adjusted to 4-5 with 2M hydrochloric acid and the precipitate was collected by filtration. The resulting solid was washed with water and dried to afford the target compound 5-methoxypyridine-2-carboxylic acid (2.4 g). The structure of the product was confirmed by 1H NMR (400 MHz, DMSO-d6): δ 3.93 (3H, s), 7.49-7.51 (1H, m), 8.03 (1H, d, J = 7.2 Hz), 8.36 (1H, d, J = 2.8 Hz), 12.85 (1H, s).

References

[1] Patent: EP2848618, 2015, A1. Location in patent: Paragraph 0707

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