1-Phenylpyrazole-4-boronic acid
1-Phenylpyrazole-4-boronic acid Basic information
- Product Name:
- 1-Phenylpyrazole-4-boronic acid
- Synonyms:
-
- 1-Phenylpyrazole-4-boronic acid
- (1-Phenyl-1H-pyrazol-4-yl)boronic acid
- 1-Phenyl-1H-pyrazole-4-boronic acid
- Boronic acid, B-(1-phenyl-1H-pyrazol-4-yl)-
- (1-phenylpyrazol-4-yl)boronic acid
- 1-Phenyl-1H-pyrazole-4-boronicacid (contains varying amounts of Anhydride)
- 1-phenypyrazole-4-boronic acid
- CAS:
- 1201643-70-0
- MF:
- C9H9BN2O2
- MW:
- 187.99
- Mol File:
- 1201643-70-0.mol
1-Phenylpyrazole-4-boronic acid Chemical Properties
- Boiling point:
- 393.1±34.0 °C(Predicted)
- Density
- 1.20±0.1 g/cm3(Predicted)
- storage temp.
- Inert atmosphere,Store in freezer, under -20°C
- pka
- 7.44±0.10(Predicted)
- Appearance
- White to yellow Solid
1-Phenylpyrazole-4-boronic acid Usage And Synthesis
Definition
ChEBI: (1-Phenyl-1H-pyrazol-4-yl)boronic acid is a ring assembly and a member of pyrazoles.
Synthesis
1002334-12-4
1201643-70-0
General procedure for the synthesis of 1-phenyl-1H-pyrazole-4-boronic acid pinacol ester from 1-phenyl-1H-pyrazole-4-boronic acid pinacol ester: To a solution of 1-phenyl-1H-pyrazole-4-boronic acid pinacol ester (0.6 g, 3.1 mmol) in acetone/water (30 mL, v/v = 1:1) was added sodium periodate (NaIO4, 2.0 g, 9.3 mmol) and ammonium acetate (NH4OAc, 0.54 g, 7.1 mmol). The reaction mixture was stirred at room temperature overnight. After completion of the reaction, the mixture was concentrated to give a residue. The residue was purified by column chromatography (eluent: methanol/dichloromethane = 1:5) to afford the target product 1-phenyl-1H-pyrazole-4-boronic acid (0.3 g, 89% yield) as a light yellow solid. Mass spectrometry (MS) analysis showed a molecular ion peak (m/z) of 189 ([M+H]+).
References
[1] Patent: WO2009/155527, 2009, A2. Location in patent: Page/Page column 134-135
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