5-Fluoro-3-iodo-1H-indazole is a heterocyclic compound characterized by the presence of both fluorine and iodine substituents on the indazole ring system. This compound features a fused bicyclic structure consisting of a five-membered pyrazole ring and a six-membered benzene ring, which contributes to its aromatic properties. The presence of the fluorine atom typically enhances the compound's lipophilicity and may influence its biological activity, while the iodine atom can provide unique reactivity due to its larger size and lower electronegativity. 5-Fluoro-3-iodo-1H-indazole is of interest in medicinal chemistry and drug development, particularly for its potential applications in targeting specific biological pathways. Its molecular structure allows for various synthetic modifications, making it a versatile scaffold in the design of new pharmaceuticals. Additionally, the compound's stability and solubility characteristics can be influenced by the substituents on the indazole ring, which are crucial for its performance in biological assays and therapeutic applications.

5-Fluoro-3-iodo-1H-indazole

858629-06-8: 5-Fluoro-3-iodo-1H-indazole is a heterocyclic compound characterized by the presence of both fluorine and iodine substituents on the indazole ring system. This compound features a fused bicyclic structure consisting of a five-membered pyrazole ring and a six-membered benzene ring, which contributes to its aromatic properties. The presence of the fluorine atom typically enhances the compound's lipophilicity and may influence its biological activity, while the iodine atom can provide unique reactivity due to its larger size and lower electronegativity. 5-Fluoro-3-iodo-1H-indazole is of interest in medicinal chemistry and drug development, particularly for its potential applications in targeting specific biological pathways. Its molecular structure allows for various synthetic modifications, making it a versatile scaffold in the design of new pharmaceuticals. Additionally, the compound's stability and solubility characteristics can be influenced by the substituents on the indazole ring, which are crucial for its performance in biological assays and therapeutic applications.

CAS 858629-06-8

5-Fluoro-3-iodo-1H-indazole

5-Fluoro-3-iodo-1H-indazole

Ref: IN-DA004XDR

5-Fluoro-3-iodo-1H-indazole

Ref: 54-PC8399

5-Fluoro-3-iodo-1H-indazole

Ref: 10-F079974