Basic information Uses Safety Supplier Related

3-METHYL-1H-PYRAZOLE-4-CARBALDEHYDE

Basic information Uses Safety Supplier Related

3-METHYL-1H-PYRAZOLE-4-CARBALDEHYDE Basic information

Product Name:
3-METHYL-1H-PYRAZOLE-4-CARBALDEHYDE
Synonyms:
  • 3-Methylpyrazole-4-carboxaldehyde
  • 4-Formyl-3-methyl-1H-pyrazole
  • 3-Methyl-1H-pyrazol-4-carbaldehyde
  • 1-Methyl Pyrazole-4-Aldehyde
  • 3-Methylpyrazole-4-carbaldehyde
  • 3-Methyl-1H-pyrazole-4-carboxaldehyde95%
  • 1H-Pyrazole-4-carboxaldehyde, 3-methy
  • 1H-Pyrazole-4-carboxaldehyde,3-Methyl-
CAS:
112758-40-4
MF:
C5H6N2O
MW:
110.11
Product Categories:
  • ALDEHYDE
  • Aldehydes
  • Pyrazoles & Triazoles
  • Pyrazoles & Triazoles
Mol File:
112758-40-4.mol
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3-METHYL-1H-PYRAZOLE-4-CARBALDEHYDE Chemical Properties

Melting point:
107-108.5°C
Boiling point:
295.9±20.0 °C(Predicted)
Density 
1.238±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
pka
12.21±0.50(Predicted)
form 
powder to crystal
color 
White to Orange to Green
InChIKey
NWDMGTFNIOCVDU-UHFFFAOYSA-N
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
22-36/37/38
Safety Statements 
26-37
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
29331990
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3-METHYL-1H-PYRAZOLE-4-CARBALDEHYDE Usage And Synthesis

Uses

3-Methyl-1H-pyrrole-4-carboxaldehyde is an aldehyde derivative that can be used as an intermediate in organic synthesis.

Synthesis

68-12-2

110-20-3

112758-40-4

N,N-dimethylformamide (65 mL) was cooled at 0 °C and trichlorophosphorus (39 mL) was slowly added dropwise over a period of 30 minutes and stirring was continued at 0 °C for 1 hour. Subsequently, 2-(propane-2-ylidene)hydrazinecarboxamide (13 g, 114 mmol) was added in batches at 0 °C, and then the reaction mixture was warmed up to 70 °C and kept for 4 hours. Upon completion of the reaction, the mixture was poured into crushed ice (500 g) and neutralized to neutral with 10% sodium hydroxide solution, followed by extraction with ethyl acetate (3 x 150 mL). The organic phases were combined, washed sequentially with water (2 x 100 mL) and saturated aqueous sodium chloride solution (100 mL), dried over anhydrous sodium sulfate and concentrated to give the crude product. The crude product was purified by column chromatography (60-120 mesh silica gel), using chloroform solution containing 2-4% methanol as eluent, and finally 3-methyl-1H-pyrazole-4-carboxaldehyde (4 g, 32% yield) was obtained as solid. The product was characterized by 1H NMR (CDCl3): δ 9.96 (s, 1H), 8.0 (s, 1H), 2.6 (s, 3H).

References

[1] Patent: WO2009/144554, 2009, A1. Location in patent: Page/Page column 37
[2] Synthesis, 1997, # 10, p. 1140 - 1142

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