1H-Indazole-5-carbonitrile is an organic compound characterized by its indazole core, which consists of a five-membered ring containing two nitrogen atoms. The presence of a cyano group (-C≡N) at the 5-position of the indazole structure contributes to its chemical reactivity and potential applications in various fields, including pharmaceuticals and agrochemicals. This compound typically exhibits a solid state at room temperature and is known for its stability under standard conditions. Its molecular structure allows for various functionalization possibilities, making it a versatile intermediate in synthetic organic chemistry. Additionally, 1H-indazole-5-carbonitrile may exhibit biological activity, which has led to interest in its potential as a lead compound in drug discovery. The compound is soluble in polar organic solvents, and its properties can be influenced by the presence of substituents on the indazole ring. Overall, 1H-indazole-5-carbonitrile is a significant compound in the realm of heterocyclic chemistry, with implications for both research and industrial applications.

1H-indazole-5-carbonitrile

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1H-Indazole-5-carbonitrile

1H-Indazole-5-carbonitrile is a synthetic organic compound with the chemical formula C7H4N2. It is an isomer of indazoles, which are heterocyclic compounds composed of a 5-member ring containing one nitrogen and four carbon atoms. 1H-Indazole-5-carbonitrile is used as a catalyst for the transfer reaction in ionic liquids. This chemical also has been shown to be an effective phase transfer catalyst for alkylation reactions. The cyano group on this molecule can react with hydrogen to form cyanohydrins and ammonia.

CAS 74626-47-4: 1H-indazole-5-carbonitrile

1H-Indazole-5-carbonitrile

Ref: 10-F063312

1H-Indazole-5-carbonitrile

Ref: 3D-FI51406

1H-Indazole-5-carbonitrile

Ref: IN-DA008PHS

1H-INDAZOLE-5-CARBONITRILE

Ref: 10-F793203

1H-Indazole-5-carbonitrile

Ref: 54-OR30733