1H-INDOLE-3-CARBOXYLIC ACID HYDRAZIDE
1H-INDOLE-3-CARBOXYLIC ACID HYDRAZIDE Basic information
- Product Name:
- 1H-INDOLE-3-CARBOXYLIC ACID HYDRAZIDE
- Synonyms:
-
- TIMTEC-BB SBB009151
- 1H-INDOLE-3-CARBOXYLIC ACID HYDRAZIDE
- 1H-INDOLE-3-CARBOHYDRAZIDE
- ART-CHEM-BB B000103
- BUTTPARK 148\07-47
- CHEMBRDG-BB 3000103
- 1H-indole-3-carbohydrazide(SALTDATA: FREE)
- Indole-3-carboxylic acid hydrazide
- CAS:
- 15317-58-5
- MF:
- C9H9N3O
- MW:
- 175.19
- Mol File:
- 15317-58-5.mol
1H-INDOLE-3-CARBOXYLIC ACID HYDRAZIDE Chemical Properties
- Melting point:
- 224-226 °C (decomp)
- Density
- 1.353±0.06 g/cm3(Predicted)
- storage temp.
- Sealed in dry,Room Temperature
- solubility
- DMSO (Sparingly), Ethanol (Slightly, Heated, Sonicated)
- form
- Solid
- pka
- 13.07±0.30(Predicted)
- color
- Pale Yellow to Pale Beige
1H-INDOLE-3-CARBOXYLIC ACID HYDRAZIDE Usage And Synthesis
Synthesis
942-24-5
15317-58-5
GENERAL PROCEDURE: Methyl indole-3-carboxylate (5 mmol) was slowly added to hydrazine hydrate (80%, 3 mL) at room temperature. Subsequently, the reaction mixture was subjected to continuous microwave irradiation at 300 W for 5-8 min. The reaction process was monitored by thin layer chromatography (TLC). Once the reaction was complete, the mixture was cooled sufficiently to room temperature to afford the intermediate indole-3-carbohydrazide in 83-98% yield.
References
[1] Journal of Chemical Research, 2015, vol. 39, # 5, p. 296 - 299
[2] European Journal of Medicinal Chemistry, 2013, vol. 63, p. 22 - 32
[3] Chemistry of Heterocyclic Compounds, 1982, vol. 18, # 3, p. 258 - 261
[4] Pharmazie, 2017, vol. 72, # 12, p. 707 - 713
[5] Chemistry of Heterocyclic Compounds, 2009, vol. 45, # 10, p. 1270 - 1275
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1H-INDOLE-3-CARBOXYLIC ACID HYDRAZIDE(15317-58-5)Related Product Information
- Indole-5-carboxaldehyde
- Indole-3-carboxaldehyde
- Indole-4-carboxaldehyde
- Indole-4-carboxylic acid
- Methyl 1H-indole-7-carboxylate
- Indole-3-glyoxylic acid
- Isatin
- Indole-6-boronic acid pinacol ester
- methyl indoline-5-carboxylate
- 6-ETHOXYCARBONYLINDOLE-2-CARBOXYLIC ACID ETHYL ESTER
- Indole-6-carboxaldehyde
- Ethyl 3-indoleacetate
- 1H-Indole-7-carboxylic acid
- Boronic acid, B-(2,3-dihydro-1H-indol-6-yl)-
- ETHYL INDOLE-2-ACETATE
- Methyl indole-6-carboxylate
- 2,3-DIHYDROINDOL-5-OL
- INDOLIN-4-AMINE