Indazole
From Wikipedia, the free encyclopedia
Indazole | |
---|---|
IUPAC name 1H-indazole | |
Identifiers | |
CAS number | 271-44-3 |
PubChem | 9221 |
ChemSpider | 8866 |
ChEBI | CHEBI:36670 |
ChEMBL | CHEMBL86795 |
Jmol-3D images | Image 1 |
| |
| |
Properties | |
Molecular formula | C7H6N2 |
Molar mass | 118.14 g/mol |
Melting point | 147-149 °C |
Boiling point | 270 °C |
(verify) (what is: / ?) Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa) | |
Infobox references | |
Indazole, also called benzpyrazole or isoindazone, is a heterocyclic aromatic organic compound.
Indazole derivatives display a broad variety of biological activities.
Indazoles are rare in Nature. The alkaloids Nigellicine, Nigeglanine, and Nigellidine are indazoles. Nigellicine was isolated from the widely distributed plant Nigella sativa L. (black cumin). Nigeglanine was isolated from extracts of Nigella glandulifera.
See also
- Indole, an analog with only one nitrogen atom in position 1.
- Benzimidazole, an analog with the nitrogen atoms in positions 1 and 3.
- Simple aromatic rings
- 7-Nitroindazole, an indazole-based nitric oxide synthase inhibitor
References
- Synthesis: W. Stadlbauer, in Science of Synthesis 2002, 12, 227, and W. Stadlbauer, in Houben-Weyl, 1994, E8b, 764.
- Review: A. Schmidt, A. Beutler, B. Snovydovych, Recent Advances in the Chemistry of Indazoles, Eur. J. Org. Chem. 2008, 4073 – 4095.
This article is issued from Wikipedia. The text is available under the Creative Commons Attribution/Share Alike; additional terms may apply for the media files.