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2-Bromopyridine-4-carboxylic acid

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2-Bromopyridine-4-carboxylic acid Basic information

Product Name:
2-Bromopyridine-4-carboxylic acid
Synonyms:
  • IFLAB-BB F1926-0035
  • 2-BROMOPYRIDINE-4-CARBOXYLIC ACID
  • 2-BROMOISONICOTINIC ACID
  • 2-BROMO-4-PYRIDINECARBOXYLIC ACID
  • 4-PYRIDINECARBOXYLIC ACID, 2-BROMO-
  • RARECHEM AL BE 1524
  • 2-bromo-4-picolinic acid
  • 2-BROMO-4-PYRIDINECARBOXYLIC ACID / 2-BROMOISONICOTINIC ACID
CAS:
66572-56-3
MF:
C6H4BrNO2
MW:
202.01
EINECS:
626-472-3
Product Categories:
  • Heterocycle-Pyridine series
  • Picolinic acid series
  • blocks
  • Bromides
  • Carboxes
  • Pyridines
  • pyridine derivative
  • pharmacetical
  • Carboxylic Acids
  • Pyridine
  • Carboxylic Acids
Mol File:
66572-56-3.mol
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2-Bromopyridine-4-carboxylic acid Chemical Properties

Melting point:
229-231°C
Boiling point:
447.2±30.0 °C(Predicted)
Density 
1.813±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
pka
2.98±0.10(Predicted)
form 
Crystals or Crystalline Powder
color 
White
BRN 
471895
InChI
InChI=1S/C6H4BrNO2/c7-5-3-4(6(9)10)1-2-8-5/h1-3H,(H,9,10)
InChIKey
YBTKGKVQEXAYEM-UHFFFAOYSA-N
SMILES
C1(Br)=NC=CC(C(O)=O)=C1
CAS DataBase Reference
66572-56-3(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36-36/37
WGK Germany 
3
Hazard Note 
Irritant/Keep Cold
HazardClass 
IRRITANT
HS Code 
29333990

MSDS

  • Language:English Provider:ALFA
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2-Bromopyridine-4-carboxylic acid Usage And Synthesis

Chemical Properties

White to light brown powder

Uses

2-Bromoisonicotinic acid (CAS 66572-56-3) is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

Application

2-Bromopyridine-4-carboxylic acid is a kind of Pyridine carboxylic acid compounds, it can be used in medicine synthesis.

Health Hazard

Accidental contact with 2-Bromopyridine-4-carboxylic acid causes skin irritation and serious eye irritation.

Synthesis

4926-28-7

66572-56-3

General procedure for the synthesis of 2-bromo-4-pyridinecarboxylic acid from 2-bromo-4-methylpyridine: To a stirred solution of 29.0 g (69 mmol) of 2-bromo-4-methylpyridine dissolved in 150 mL of concentrated sulfuric acid was added batchwise 67.9 g (231 mmol) of potassium dichromate. The reaction was cooled using an ice bath to maintain a constant temperature. After addition, the reaction mixture was continued to be stirred at room temperature for 2 hours. Subsequently, the reaction mixture was slowly poured into 2 L of ice water and stirred at room temperature for 1 hour. The resulting crystals were collected by filtration, washed with water until the eluent was colorless, and finally dried under vacuum to give 30.0 g (88% yield) of 2-bromo-4-pyridinecarboxylic acid.

References

[1] Patent: US2011/111046, 2011, A1. Location in patent: Page/Page column 17; 18
[2] Patent: WO2011/58473, 2011, A1. Location in patent: Page/Page column 36; 37
[3] Chemical and Pharmaceutical Bulletin, 1990, vol. 38, # 9, p. 2446 - 2458
[4] Patent: US2008/51397, 2008, A1. Location in patent: Page/Page column 9; 24
[5] Polyhedron, 2016, vol. 118, p. 159 - 170

2-Bromopyridine-4-carboxylic acid Preparation Products And Raw materials

Raw materials

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