Basic information Safety Supplier Related

5-METHYL-1H-PYRAZOLE-4-CARBOXYLIC ACID METHYL ESTER

Basic information Safety Supplier Related

5-METHYL-1H-PYRAZOLE-4-CARBOXYLIC ACID METHYL ESTER Basic information

Product Name:
5-METHYL-1H-PYRAZOLE-4-CARBOXYLIC ACID METHYL ESTER
Synonyms:
  • 5-METHYL-1H-PYRAZOLE-4-CARBOXYLIC ACID METHYL ESTER
  • Methyl 3-Methyl-1H-pyrazole-4-carboxylate
  • Methyl 5-Methyl-1H-pyrazole-4-carboxylate
  • Methyl 3-Methylpyrazole-4-carboxylate
  • 3-Cyclopentyl-1H-pyrazole-4-carboxylic acid methyl ester
  • 1H-Pyrazole-4-carboxylic acid, 3-methyl-, methyl ester
  • Methyl 3-methyl-1H-pyrazol-4-carboxylate
CAS:
23170-45-8
MF:
C6H8N2O2
MW:
140.14
Mol File:
23170-45-8.mol
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5-METHYL-1H-PYRAZOLE-4-CARBOXYLIC ACID METHYL ESTER Chemical Properties

Boiling point:
268.5±20.0 °C(Predicted)
Density 
1.217±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
pka
12.15±0.50(Predicted)
Appearance
Light yellow to yellow Solid
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Safety Information

HS Code 
2933199090
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5-METHYL-1H-PYRAZOLE-4-CARBOXYLIC ACID METHYL ESTER Usage And Synthesis

Uses

methyl 3-methyl-1h-pyrazole-4-carboxylate is used in the preparation of triazines and their phosphorus analogs via cyclization, ring transformation, aromatization, and substituent modification.

Synthesis

67-56-1

40704-11-8

23170-45-8

General procedure for the synthesis of ethyl 3-methyl-1H-pyrazole-4-carboxylate from methanol and 3-methylpyrazole-4-carboxylic acid: 3-methylpyrazole-4-carboxylic acid (1.26 g, 10 mmol) was dissolved in methanol (100 mL) at 0 °C and thionyl chloride (5.73 g, 45 mmol) was added slowly, the reaction mixture was stirred at room temperature for 12 hours. After completion of the reaction, the solvent was removed by vacuum evaporation. The residue was neutralized by adding saturated aqueous sodium bicarbonate solution and the mixture was extracted with ethyl acetate (100 mL x 3). The organic phases were combined, dried with anhydrous sodium sulfate, filtered and the filtrate was concentrated in vacuum to give ethyl 3-methyl-1H-pyrazole-4-carboxylate (0.8 g, 57% yield). The product was characterized by 1H NMR (300 MHz, CDCl3): δ 7.87 (s, 1H), 3.84 (s, 3H), 2.53 (s, 3H).

References

[1] Patent: WO2013/120104, 2013, A2. Location in patent: Paragraph 00183; 00184
[2] Bioorganic and Medicinal Chemistry Letters, 2015, vol. 25, # 17, p. 3644 - 3649
[3] Advanced Synthesis and Catalysis, 2010, vol. 352, # 11-12, p. 2041 - 2049

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