Basic information Safety Supplier Related

METHYL 2-BROMO-5-FLUOROISONICOTINATE

Basic information Safety Supplier Related

METHYL 2-BROMO-5-FLUOROISONICOTINATE Basic information

Product Name:
METHYL 2-BROMO-5-FLUOROISONICOTINATE
Synonyms:
  • METHYL 2-BROMO-5-FLUOROISONICOTINATE
  • Methyl 2-broMo-5-fluoropyridine-4-carboxylate
  • Methyl 2-bromo-5-fluoropyridine-4-carboxylate, 2-Bromo-5-fluoro-4-(methoxycarbonyl)pyridine
  • Methy 2-broMo-5-fluoropyridine-4-carboxylate
  • 4-pyridinecarboxylic acid, 2-bromo-5-fluoro-, methyl ester
  • 2-Bromo-5-fluoro-isonicotinic acid methyl ester
  • 3-Fluoro-2-methoxy-7-(trifluoromethyl)pyridine
CAS:
885588-14-7
MF:
C7H5BrFNO2
MW:
234.02
Mol File:
885588-14-7.mol
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METHYL 2-BROMO-5-FLUOROISONICOTINATE Chemical Properties

Boiling point:
264.0±40.0 °C(Predicted)
Density 
1.660±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
-3.76±0.18(Predicted)
form 
crystalline needles
color 
Off-white
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Safety Information

HS Code 
2933399990
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METHYL 2-BROMO-5-FLUOROISONICOTINATE Usage And Synthesis

Synthesis

67-56-1

885588-12-5

885588-14-7

To a stirred solution of 2-bromo-5-fluoropyridine-4-carboxylic acid (2.8 g, 12.78 mmol) in methanol (30 ml) was slowly added thionyl chloride (7.54 g, 63.9 mmol) at room temperature. The reaction mixture was stirred continuously for 16 hours at room temperature. After completion of the reaction, the solvent was removed by concentration under reduced pressure. The residue was dissolved in water (100 ml) and the pH was adjusted with saturated sodium bicarbonate solution to 8. Subsequently, extraction was carried out with ethyl acetate (2 x 100 ml). The organic layers were combined, dried with anhydrous sodium sulfate, filtered and concentrated under reduced pressure to give methyl 2-bromo-5-fluoroisonicotinate (2.2 g, 73% yield) as a light yellow solid. The results were analyzed by liquid chromatography-mass spectrometry (Method 8): retention time (Rt) = 2.41 min; mass-to-charge ratio (m/z) = 234.07 ([M+H]+).

References

[1] Patent: WO2006/45514, 2006, A1. Location in patent: Page/Page column 38
[2] Patent: WO2017/207813, 2017, A1. Location in patent: Page/Page column 150

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