Indazole

Indazole

Skeletal formula with numbering convention
Ball-and-stick model Space-filling model
Names
IUPAC name 1H-indazole
Identifiers
CAS Number	271-44-3 Y
ChEBI	CHEBI:36670 Y
ChEMBL	ChEMBL86795 Y
ChemSpider	8866 Y
Jmol 3D model	Interactive image
PubChem	9221
InChI InChI=1S/C7H6N2/c1-2-4-7-6(3-1)5-8-9-7/h1-5H,(H,8,9) Y Key: BAXOFTOLAUCFNW-UHFFFAOYSA-N Y InChI=1/C7H6N2/c1-2-4-7-6(3-1)5-8-9-7/h1-5H,(H,8,9) Key: BAXOFTOLAUCFNW-UHFFFAOYAQ
SMILES n2cc1ccccc1n2
Properties
Chemical formula	C7H6N2
Molar mass	118.14 g/mol
Melting point	147 to 149 °C (297 to 300 °F; 420 to 422 K)
Boiling point	270 °C (518 °F; 543 K)
Vapor pressure	{{{value}}}
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Y verify (what is YN ?)
Infobox references

Indazole, also called isoindazole, is a heterocyclic aromatic organic compound. This bicyclic compound consists of the fusion of benzene and pyrazole.

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. The Davis–Beirut reaction can generate 2H-indazoles.

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.