5-Nitroindazole-3-carboxylic acid
5-Nitroindazole-3-carboxylic acid Basic information
- Product Name:
- 5-Nitroindazole-3-carboxylic acid
- Synonyms:
-
- 5-NITRO INDAZOLE CARBOXYLIC ACID
- 5-NITRO-3-(1H)INDAZOLE CARBOXYLIC ACID
- 5-NITRO-1H-INDAZOLE-3-CARBOXYLIC ACID
- Nitro indazole carboxylic acid (70%)
- 1H-Indazole-3-carboxylic acid, 5-nitro-
- Nitro indazole carboxylic acid
- 5-NITROINDAZOLE-3-CARBOXYLIC ACID
- CAS:
- 78155-76-7
- MF:
- C8H5N3O4
- MW:
- 207.14
- Mol File:
- 78155-76-7.mol
5-Nitroindazole-3-carboxylic acid Chemical Properties
- Melting point:
- 280 °C(Solv: acetic acid (64-19-7))
- Boiling point:
- 547.1±30.0 °C(Predicted)
- Density
- 1.733±0.06 g/cm3(Predicted)
- storage temp.
- 2-8°C
- pka
- 2.51±0.30(Predicted)
- Appearance
- Light yellow to yellow Solid
5-Nitroindazole-3-carboxylic acid Usage And Synthesis
Synthesis
677702-36-2
78155-76-7
The general procedure for the synthesis of 5-nitroindazole-3-carboxylic acid from 5-nitroindazole-3-aldehyde was as follows: potassium permanganate (KMnO4, 15 g, 94.91 mmol) was dissolved in 300 mL of water and added slowly and dropwise at room temperature to 1000 mL of acetone solution containing 52.35 mmol of raw material. The reaction mixture was stirred at room temperature for 6 hours. Subsequently, 50 mL of 30% hydrogen peroxide (H2O2) was added dropwise to neutralize the remaining potassium permanganate. The reaction mixture was filtered to remove insoluble matter and then concentrated by distillation under reduced pressure. After acidification of the concentrate, the precipitate was collected by filtration and recrystallized from methanol to give a final 6. yellow solid product; yield 79% (8.56 g); melting point: 191-193°C.
References
[1] Monatshefte fur Chemie, 2017, vol. 148, # 2, p. 305 - 314
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