Basic information Safety Supplier Related

1-Phenyl-1H-pyrazole-4-carboxylic acid

Basic information Safety Supplier Related

1-Phenyl-1H-pyrazole-4-carboxylic acid Basic information

Product Name:
1-Phenyl-1H-pyrazole-4-carboxylic acid
Synonyms:
  • 1-phenyl-pyrazole-4-carboxylicaci
  • AKOS PAO-0321
  • ASINEX-REAG BAS 16289592
  • 1-PHENYL-1H-PYRAZOLE-4-CARBOXYLIC ACID
  • 1-phenyl-1H-pyrazole-4-carboxylic acid(SALTDATA: FREE)
  • 1-phenyl-1H-pyrazol-4-carboxylic acid
  • 1H-Pyrazole-4-carboxylic acid, 1-phenyl-
  • 1-phenyl-4-pyrazolecarboxylic acid
CAS:
1134-50-5
MF:
C10H8N2O2
MW:
188.18
EINECS:
413-030-8
Product Categories:
  • C10
  • Chemical Synthesis
  • Heterocyclic Building Blocks
  • Pyrazoles
  • Building Blocks
Mol File:
1134-50-5.mol
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1-Phenyl-1H-pyrazole-4-carboxylic acid Chemical Properties

Melting point:
222-227℃
Boiling point:
379.6±15.0 °C(Predicted)
Density 
1.28±0.1 g/cm3(Predicted)
storage temp. 
2-8°C
form 
solid
pka
3.75±0.10(Predicted)
Appearance
White to off-white Solid
CAS DataBase Reference
1134-50-5(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
WGK Germany 
1
RTECS 
UQ6436000
HazardClass 
IRRITANT
HS Code 
2933199090

MSDS

  • Language:English Provider:ALFA
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1-Phenyl-1H-pyrazole-4-carboxylic acid Usage And Synthesis

Synthesis

54605-72-0

1134-50-5

Steps: Sodium hydroxide was dissolved in a 100 mL three-neck reaction flask containing 20 mL of water under nitrogen protection and magnetic stirring. Subsequently, 1-phenyl-1H-pyrazole-4-carbaldehyde was added in one go. Persistent insoluble products were observed even at temperatures of 45-50 °C. Hydrogen peroxide was added to the suspension in six portions over a period of 50 min. After the reaction lasted for 5 h at 50 °C, monitoring by TLC showed that most of the raw material remained. Next, 10 mL of 1N NaOH solution (containing 0.4 g NaOH) and 5 g aqueous hydrogen peroxide were added. After continued stirring at 50 °C for 1 h, the insoluble product completely disappeared and TLC monitoring confirmed that the starting material had been completely consumed (color developer: dinitrophenylhydrazine). The reaction mixture was cooled to room temperature and poured into 150 mL of ice/2N HCl mixture (2:1 volume ratio). After stirring for 30 min, the white precipitate formed was filtered through a Brinell's funnel and washed three times with water. The precipitate was dissolved in 250 mL of ethyl acetate, dried over anhydrous magnesium sulfate, filtered and evaporated to dryness to give 2.25 g of white solid product (yield: 96%).

References

[1] Inflammopharmacology, 2018, vol. 26, # 1, p. 217 - 226
[2] Patent: US2006/34786, 2006, A1. Location in patent: Page/Page column 62-63
[3] Chemical and Pharmaceutical Bulletin, 1980, vol. 28, # 4, p. 1265 - 1269
[4] Patent: US2009/239810, 2009, A1. Location in patent: Page/Page column 72

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