Basic information Uses Safety Supplier Related

3-TRIFLUOROMETHYL-1H-PYRAZOLE-4-CARBALDEHYDE

Basic information Uses Safety Supplier Related

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

Product Name:
3-TRIFLUOROMETHYL-1H-PYRAZOLE-4-CARBALDEHYDE
Synonyms:
  • 3-TRIFLUOROMETHYL-1H-PYRAZOLE-4-CARBALDEHYDE
  • 3-(Trifluoromethyl)-1H-pyrazole-4-carboxaldehyde
  • 4-Formyl-3-(trifluoromethyl)-1H-pyrazole
  • 1H-Pyrazole-4-carboxaldehyde, 3-(trifluoromethyl)-
  • 5-(trifluoromethyl)-1H-pyrazole-4-carbaldehyde
CAS:
1001020-14-9
MF:
C5H3F3N2O
MW:
164.09
Product Categories:
  • Pyrazoles & Triazoles
  • Aldehydes
  • Pyrazoles & Triazoles
Mol File:
Mol File
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3-TRIFLUOROMETHYL-1H-PYRAZOLE-4-CARBALDEHYDE Chemical Properties

Boiling point:
285.7±40.0 °C(Predicted)
Density 
1.545±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
8.21±0.50(Predicted)
Appearance
White to off-white Solid
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Safety Information

HS Code 
2933199090
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3-TRIFLUOROMETHYL-1H-PYRAZOLE-4-CARBALDEHYDE Usage And Synthesis

Uses

3-(trifluoromethyl)pyrazole-4-carboxaldehyde is an aldehyde organic compound that can be used as an organic intermediate.

Synthesis

1001020-13-8

1001020-14-9

3-(Trifluoromethyl)-1H-pyrazol-4-ylmethanol (54.00 g, 0.325 mol) was used as a raw material and suspended in toluene (2 L). Manganese dioxide (113.00 g, 1.30 mol) and 4?molecular sieve powder (54.00 g) were added to the suspension. The reaction mixture was stirred at reflux for 5.5 hours under nitrogen protection, assembled with a Dean-Stark splitter. Upon completion of the reaction, the reaction mixture was filtered while hot, the filter cake was collected and cooled to room temperature. The filter cake was washed with a 1:1 mixture of dichloromethane and methanol (3 x 500 mL). All the filtrates were combined and the solvent was removed by concentration under reduced pressure to afford the target product 3-(trifluoromethyl)pyrazole-4-carbaldehyde (54.00 g, 0.329 mol, 100% yield). The product was characterized by 1H NMR (400 MHz, DMSO-d6): δ 8.72 (s, 1H), 9.91 (s, 1H).

References

[1] Patent: US2009/131455, 2009, A1. Location in patent: Page/Page column 8
[2] Patent: WO2008/3452, 2008, A1. Location in patent: Page/Page column 53

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