Basic information Safety Supplier Related

4-BROMO-1-METHYL-1 H-PYRAZOLE-3-CARBOXYLIC ACID M ETHYL ESTER

Basic information Safety Supplier Related

4-BROMO-1-METHYL-1 H-PYRAZOLE-3-CARBOXYLIC ACID M ETHYL ESTER Basic information

Product Name:
4-BROMO-1-METHYL-1 H-PYRAZOLE-3-CARBOXYLIC ACID M ETHYL ESTER
Synonyms:
  • RARECHEM AL BF 1005
  • ART-CHEM-BB B001423
  • 4-BROMO-1-METHYL-1 H-PYRAZOLE-3-CARBOXYLIC ACID M ETHYL ESTER
  • AKOS B001423
  • methyl 4-bromo-1-methyl-1H-pyrazole-3-carboxylate
  • 1H-pyrazole-3-carboxylic acid, 4-bromo-1-methyl-, methyl e
  • methyl 4-bromo-1-methyl-1H-pyrazole-3-carboxylate(SALTDATA: FREE)
  • 4-bromo-1-methyl-3-pyrazolecarboxylic acid methyl ester
CAS:
211738-66-8
MF:
C6H7BrN2O2
MW:
219.04
Mol File:
211738-66-8.mol
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4-BROMO-1-METHYL-1 H-PYRAZOLE-3-CARBOXYLIC ACID M ETHYL ESTER Chemical Properties

Boiling point:
276.5±20.0 °C(Predicted)
Density 
1.67±0.1 g/cm3(Predicted)
storage temp. 
2-8°C
pka
-2.22±0.10(Predicted)
Appearance
White to off-white Solid
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Safety Information

HazardClass 
IRRITANT
HS Code 
2933199090
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4-BROMO-1-METHYL-1 H-PYRAZOLE-3-CARBOXYLIC ACID M ETHYL ESTER Usage And Synthesis

Synthesis

81190-89-8

74-88-4

514816-42-3

211738-66-8

To a mixture of methyl 4-bromo-1H-pyrazole-3-carboxylate (15.0 g, 73.2 mmol) and Cs2CO3 (59.6 g, 182.9 mmol) in DMF (150 mL) was added slowly and dropwise at 0 °C under nitrogen protection iodomethane (14.7 mL, 236.0 mmol). The reaction mixture was stirred at 25 °C for 16 hours. After completion of the reaction, the mixture was filtered and the filter cake was washed with ethyl acetate (200 mL x 2). The combined filtrates were washed with water (70 mL x 4) and the aqueous phase was then back-extracted with ethyl acetate (150 mL). All organic phases were combined, dried with Na2SO4, filtered and concentrated to dryness under reduced pressure. The crude product was purified by fast column chromatography (gradient elution: petroleum ether/ethyl acetate from 100/0 to 50/50) to afford methyl 4-bromo-1-methyl-1H-pyrazole-3-carboxylate (240a, 8.3 g, 51.8% yield) and methyl 4-bromo-1-methyl-1H-pyrazole-5-carboxylate (240b, 7.0 g, 43.7% yield), both as white solid . 1H NMR (400 MHz, CDCl3) data for compound 240a: δ 7.48 (s, 1H), 4.15 (s, 3H), 3.93 (s, 3H). m/z (M + H) + 219.0 in MS (ESI).

References

[1] Patent: WO2018/64119, 2018, A1. Location in patent: Paragraph 1197

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