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4-METHYL-PYRIDINE-2-CARBOXYLIC ACID

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4-METHYL-PYRIDINE-2-CARBOXYLIC ACID Basic information

Product Name:
4-METHYL-PYRIDINE-2-CARBOXYLIC ACID
Synonyms:
  • 4-METHYLPICOLINIC ACID
  • 4-METHYL-PYRIDINE-2-CARBOXYLIC ACID
  • 4-Methylpyridine-2-carboxylic acid 97%
  • 4-Methylpicolinic acid ,97%
  • 4-Methylpyridine-2-carboxylic acid ,97%
  • 4-Methylpicolinic acid, 2-Carboxy-4-methylpyridine
  • 2-Pyridinecarboxylic acid, 4-methyl-
  • RARECHEM AL BO 2389
CAS:
4021-08-3
MF:
C7H7NO2
MW:
137.14
Product Categories:
  • Carboxylic Acids
  • C7 and C8
  • Heterocyclic Building Blocks
  • Heterocyclic Compounds
  • pharmacetical
  • Pyridine series
  • Carboxylic Acids
  • Pyridines
Mol File:
4021-08-3.mol
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4-METHYL-PYRIDINE-2-CARBOXYLIC ACID Chemical Properties

Melting point:
137-141 °C
Boiling point:
307.4±22.0 °C(Predicted)
Density 
1.230±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
form 
powder to crystal
pka
1.11±0.50(Predicted)
color 
White to Light yellow
CAS DataBase Reference
4021-08-3(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36/37/39-24/25
WGK Germany 
3
Hazard Note 
Irritant
HS Code 
29333990
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4-METHYL-PYRIDINE-2-CARBOXYLIC ACID Usage And Synthesis

Chemical Properties

White to light brown solid

Uses

4-Methylpyridine-2-carboxylic acid is a used in biological studies for the mutasynthesis of potential neuroprotectant derivatives of the bipyridyl collismycin A.

Synthesis

1620-76-4

4021-08-3

General procedure for the synthesis of 4-methylpyridine-2-carboxylic acid from 2-cyano-4-methylpyridine: 2-cyano-4-methylpyridine (0.15 g, 1.27 mmol) was dissolved in about 10 mL of 6 M hydrochloric acid and heated and refluxed for 24 hours. During the reaction, the solution gradually changed from the initial pale yellow color to clear. Upon completion of the reaction, the solution was evaporated to dryness to give a white solid product. Purification by recrystallization from a minimal amount of distilled water resulted in 148 mg (85% yield) of 4-methylpyridine-2-carboxylic acid. The product was characterized by 1H NMR (DMSO-d6): δ = 8.65 (1H, s), 8.06 (1H, s), 7.66 (1H, s), 2.05 (3H, s).

References

[1] Patent: WO2008/17855, 2008, A1. Location in patent: Page/Page column 49
[2] Patent: WO2008/17855, 2008, A1. Location in patent: Page/Page column 49
[3] Patent: US5219847, 1993, A
[4] Advanced Synthesis and Catalysis, 2013, vol. 355, # 5, p. 947 - 956
[5] Patent: US6251919, 2001, B1

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