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CAS 1082041-91-5

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4-Chloro-1H-indazole-5-carbonitrile

Description:
4-Chloro-1H-indazole-5-carbonitrile is a heterocyclic organic compound characterized by its indazole core, which features a chlorine atom at the 4-position and a cyano group (-C≡N) at the 5-position. This compound is typically a solid at room temperature and is known for its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals due to its bioactive properties. The presence of the cyano group contributes to its reactivity, allowing for further chemical modifications. Additionally, the chlorine substituent can influence the compound's electronic properties and solubility. 4-Chloro-1H-indazole-5-carbonitrile may exhibit various biological activities, making it a subject of interest in drug discovery and development. Its synthesis often involves multi-step organic reactions, and it is important to handle this compound with care due to potential toxicity associated with halogenated compounds. As with many indazole derivatives, it may also serve as a scaffold for the design of new therapeutic agents.
Formula:C8H4ClN3
InChI:InChI=1S/C8H4ClN3/c9-8-5(3-10)1-2-7-6(8)4-11-12-7/h1-2,4H,(H,11,12)
InChI key:InChIKey=HKLXPJOGSHCVGX-UHFFFAOYSA-N
SMILES:ClC1=C2C(=CC=C1C#N)NN=C2
Synonyms:
  • 4-Chloro-1H-indazole-5-carbonitrile
  • 1H-Indazole-5-carbonitrile, 4-chloro-
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