Basic information Safety Supplier Related

3-(4-FLUOROPHENYL)-1H-PYRAZOLE-4-CARBALDEHYDE

Basic information Safety Supplier Related

3-(4-FLUOROPHENYL)-1H-PYRAZOLE-4-CARBALDEHYDE Basic information

Product Name:
3-(4-FLUOROPHENYL)-1H-PYRAZOLE-4-CARBALDEHYDE
Synonyms:
  • AKOS B000254
  • AKOS PAO-0297
  • 3-(4-FLUOROPHENYL)-1H-PYRAZOLE-4-CARBALDEHYDE
  • 3-(4-FLUOROPHENYL)PYRAZOLE-4-CARBOXALDEHYDE
  • CHEMBRDG-BB 4301174
  • ART-CHEM-BB B000254
  • 3-(4-Fluorophenyl)-1H-pyrazole-4-carboxaldehyde
  • 3-(4-Fluorophenyl)-1H-pyrazole-4-carboxaldehyde 97%
CAS:
306936-57-2
MF:
C10H7FN2O
MW:
190.17
Product Categories:
  • Building Blocks
  • C10
  • C10-C12
  • Carbonyl Compounds
  • Chemical Synthesis
  • Fluorinated Building Blocks
  • Halogenated Heterocycles
  • Heterocyclic Building Blocks
  • Heterocyclic Fluorinated Building Blocks
  • Organic Building Blocks
  • Other Fluorinated Heterocycles
  • Aldehydes
  • Pyrazoles & Triazoles
  • Pyrazoles & Triazoles
  • Halogenated Heterocycles
  • Heterocyclic Building Blocks
  • Pyrazoles
Mol File:
306936-57-2.mol
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3-(4-FLUOROPHENYL)-1H-PYRAZOLE-4-CARBALDEHYDE Chemical Properties

Melting point:
160 °C
Boiling point:
416.0±35.0 °C(Predicted)
Density 
1.337±0.06 g/cm3(Predicted)
storage temp. 
2-8°C, stored under nitrogen
form 
powder to crystal
pka
10.69±0.50(Predicted)
color 
White to Orange to Green
Sensitive 
Air Sensitive
CAS DataBase Reference
306936-57-2(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36/37/39
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
29331990
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3-(4-FLUOROPHENYL)-1H-PYRAZOLE-4-CARBALDEHYDE Usage And Synthesis

Chemical Properties

White to yellow-orange solid

Synthesis

326-33-0

68-12-2

306936-57-2

General procedure for the synthesis of 3-(4-fluoropropyl)-1H-pyrazole-4-carbaldehyde from 2-(1-(4-fluorophenyl)ethylidene)hydrazine-1-carboxamide and N,N-dimethylformamide: Phosphorochloride (2.1 mL, 23 mmol) was slowly added dropwise to N,N-dimethylformamide (4.4 mL, 57 mmol) at 0 °C. The reaction mixture was stirred at 0 °C for 30 min, then brought to room temperature and continued stirring for 30 min. Subsequently, the reaction mixture was cooled in an ice/water bath and 2-(1-(4-fluorophenyl)ethylidene)hydrazine-1-carboxamide (1.96 g, 10 mmol) was slowly added, controlling the temperature not to exceed 50 °C. After the addition was completed, the reaction system was heated to 80 °C and stirred at this temperature for 2 hours. After completion of the reaction, the mixture was poured into ice (15 g) and the pH was adjusted to 10 with 5N NaOH solution and stirred for 2 hours. Subsequently, the reaction solution was acidified with concentrated hydrochloric acid and stirring was continued for 4 hours. The precipitated solid was collected by filtration, washed with a small amount of water and dried under high vacuum to give the target product 3-(4-fluoropropyl)-1H-pyrazole-4-carbaldehyde (1.5 g, 79% yield).

References

[1] Bioorganic and Medicinal Chemistry Letters, 2008, vol. 18, # 18, p. 4932 - 4935
[2] Russian Journal of General Chemistry, 2005, vol. 75, # 5, p. 782 - 789
[3] Patent: WO2013/22766, 2013, A1. Location in patent: Page/Page column 87
[4] European Journal of Medicinal Chemistry, 2017, vol. 133, p. 36 - 49
[5] Journal of Fluorine Chemistry, 2016, vol. 183, p. 59 - 68

3-(4-FLUOROPHENYL)-1H-PYRAZOLE-4-CARBALDEHYDE Preparation Products And Raw materials

Raw materials

3-(4-FLUOROPHENYL)-1H-PYRAZOLE-4-CARBALDEHYDESupplier

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