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3-BROMOISONICOTINIC ACID METHYL ESTER

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3-BROMOISONICOTINIC ACID METHYL ESTER Basic information

Product Name:
3-BROMOISONICOTINIC ACID METHYL ESTER
Synonyms:
  • 3-BROMOISONICOTINIC ACID METHYL ESTER
  • 3-BROMOPYRIDINE-4-CARBOXYLIC ACID METHYL ESTER
  • Methyl 3-bromopyridine-4-carboxylate
  • 3-broMopyridin-4-carboxylic acid Methyl ester
  • Methyl-3-broMoisonicotiMate
  • 3-broMopyridine-4-carboxylate
  • Methyl 3-bromo-4-pyridinecarboxylate
  • Methyl 3-bromoisonicotinate
CAS:
59786-31-1
MF:
C7H6BrNO2
MW:
216.03
Product Categories:
  • blocks
  • Bromides
  • Carboxes
  • Pyridines
  • Building Blocks
  • Pyridine
Mol File:
59786-31-1.mol
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3-BROMOISONICOTINIC ACID METHYL ESTER Chemical Properties

Boiling point:
247℃
Density 
1.579
refractive index 
1.56
Flash point:
103℃
storage temp. 
Inert atmosphere,Room Temperature
form 
clear liquid
pka
0.76±0.18(Predicted)
color 
Colorless to Yellow to Orange
CAS DataBase Reference
59786-31-1
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Safety Information

Hazard Codes 
Xi
HazardClass 
IRRITANT
HS Code 
2933399990
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3-BROMOISONICOTINIC ACID METHYL ESTER Usage And Synthesis

Uses

Methyl 3-bromoisonicotinate is an important chemical reagent, mainly used as organic synthesis or pharmaceutical intermediates for the preparation of compounds such as alkaloids, tricyclic compounds or small molecule enzyme inhibitors.

Synthesis

67-56-1

13959-02-9

59786-31-1

3.98 g (20 mmol, 1 eq.) of 3-bromoisonicotinic acid was dissolved in 50 ml of methanol and 4 ml of concentrated sulfuric acid was added as catalyst. The reaction mixture was heated to reflux. After completion of the reaction, it was cooled to room temperature and extracted three times with ethyl acetate. The organic phases were combined, dried over anhydrous sodium sulfate and concentrated under reduced pressure to remove the solvent. 2.65 g (62% yield) of methyl 3-bromoisonicotinate was obtained. The structure of the product was confirmed by 1H NMR (CDCl3): δ 4.02 (s, 3H), 7.64 (d, J = 4.9 Hz, 1H), 8.63 (d, J = 4.9 Hz, 1H), 8.88 (s, 1H).

References

[1] Patent: US2005/80085, 2005, A1. Location in patent: Page/Page column 12
[2] Patent: US2010/130477, 2010, A1. Location in patent: Page/Page column 58
[3] Patent: US2011/230495, 2011, A1. Location in patent: Page/Page column 23-24
[4] Advanced Synthesis and Catalysis, 2016, vol. 358, # 20, p. 3283 - 3292

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