1-Phenyl-1H-pyrazole-4-carboxylic acid
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
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)
Safety Information
- Hazard Codes
- Xi
- WGK Germany
- 1
- RTECS
- UQ6436000
- HazardClass
- IRRITANT
- HS Code
- 2933199090
MSDS
- Language:English Provider:ALFA
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
1-Phenyl-1H-pyrazole-4-carboxylic acidSupplier
- Tel
- 18210857532; 18210857532
- jkinfo@jkchemical.com
- Tel
- 400-6106006
- saleschina@alfa-asia.com
- Tel
- 021-021-58432009 400-005-6266
- sales8178@energy-chemical.com
- Tel
- +86 (0) 571 85 58 67 18
- Tel
- 001-857-928-2050 or 1-888-588-9418
- sales@chemreagents.com
1-Phenyl-1H-pyrazole-4-carboxylic acid(1134-50-5)Related Product Information
- Pyraclostrobin
- Pyrazole
- Zolpidem tartrate
- PHENYL VALERATE
- Diphenyl ether
- 5-Methyl-2-phenyl-1,2-dihydropyrazol-3-one
- Phenyl salicylate
- PHENYL RESIN
- 5-METHYL-1-PHENYL-1H-PYRAZOLE-4-CARBOXYLIC ACID
- 1-PHENYL-5-PROPYL-1H-PYRAZOLE-4-CARBOXYLIC ACID
- Zolpidem
- 1-(4-CHLOROPHENYL)-5-PROPYL-1H-PYRAZOLE-4-CARBOXYLIC ACID
- ETHYL 2-PHENYL-3-(TRIFLUOROMETHYL)PYRAZOLE-4-CARBOXYLATE
- ETHYL 5-METHYL-1-PHENYL-1H-PYRAZOLE-4-CARBOXYLATE
- 5-AMINO-4-CARBETHOXY-1-PHENYLPYRAZOLE
- Phenylacetic acid
- 5-(3-HYDROXY-PHENYL)-1H-PYRAZOLE-3-CARBOXYLIC ACID
- Sodium 5-oxo-1-(4-sulfophenyl)-4H-pyrazole-3-carboxylate