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ChemicalBook >  Product Catalog >  Organic Chemistry >  Carboxylic acids and derivatives >  Carboxylic acid esters and derivatives >  5-HYDROXY-1-METHYL-1H-PYRAZOLE-3-CARBOXYLIC ACID METHYL ESTER

5-HYDROXY-1-METHYL-1H-PYRAZOLE-3-CARBOXYLIC ACID METHYL ESTER

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5-HYDROXY-1-METHYL-1H-PYRAZOLE-3-CARBOXYLIC ACID METHYL ESTER Basic information

Product Name:
5-HYDROXY-1-METHYL-1H-PYRAZOLE-3-CARBOXYLIC ACID METHYL ESTER
Synonyms:
  • 1-Methyl-5-oxo-2,5-dihydro-1H-pyrazole-3-carboxylic acid methyl ester
  • Methyl 5-hydroxy-1-methyl-1H-pyrazole-3-carboxylate 97%
  • Methyl 5-hydroxy-1-methyl-3-pyrazolecarboxylate
  • NSC 338308
  • 5-HYDROXY-1-METHYL-1H-PYRAZOLE-3-CARBOXYLIC ACID METHYL ESTER
  • 1H-Pyrazole-3-carboxylic acid, 1-methyl-, methyl ester
  • Methyl 5-hydroxy-1-Methyl-1H-pyrazole-3-carboxylate
  • Methyl 1-Methyl-5-oxo-2,5-dihydro-1H-pyrazole-3-carboxylate
CAS:
51985-95-6
MF:
C6H8N2O3
MW:
156.14
Mol File:
51985-95-6.mol
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5-HYDROXY-1-METHYL-1H-PYRAZOLE-3-CARBOXYLIC ACID METHYL ESTER Chemical Properties

Melting point:
195-200°C
Boiling point:
330.7±22.0 °C(Predicted)
Density 
1.35±0.1 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
form 
solid
pka
8.26±0.28(Predicted)
color 
Pale brown
InChI
InChI=1S/C6H8N2O3/c1-8-5(9)3-4(7-8)6(10)11-2/h3,9H,1-2H3
InChIKey
IWOKRTHKTAEDLP-UHFFFAOYSA-N
SMILES
N1(C)C(O)=CC(C(OC)=O)=N1
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Safety Information

WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
2933199090
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5-HYDROXY-1-METHYL-1H-PYRAZOLE-3-CARBOXYLIC ACID METHYL ESTER Usage And Synthesis

Synthesis

58364-79-7

51985-95-6

b) Methyl 5-hydroxy-1-methyl-1H-pyrazole-3-carboxylate (12.2 g, 65 mmol) was dissolved in xylene (65 mL) and p-toluenesulfonic acid (0.9 g, 4.7 mmol) was added. The reaction mixture was heated to reflux for 6 hours. Upon completion of the reaction, it was cooled to room temperature and stirred overnight. The precipitated solid was collected by filtration and dissolved in ethyl acetate. The organic phase was washed sequentially with sodium bicarbonate solution and saturated brine and dried over anhydrous sodium sulfate. After filtration, the organic phase was concentrated under reduced pressure to give methyl 1-methyl-5-hydroxypyrazole-3-carboxylate (7.49 g, 74% yield) as a light brown solid. The purity of the product was improved by diisopropyl ether milling. Mass spectrometry analysis showed: m/e = 157.2 [M + H]+.

References

[1] Patent: WO2010/127975, 2010, A1. Location in patent: Page/Page column 131

5-HYDROXY-1-METHYL-1H-PYRAZOLE-3-CARBOXYLIC ACID METHYL ESTER Supplier

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