7-Bromo-1H-indazol-5-ol is a chemical compound characterized by its indazole core, which is a five-membered heterocyclic structure containing two nitrogen atoms. The presence of a bromine atom at the 7-position and a hydroxyl group (-OH) at the 5-position contributes to its unique reactivity and potential applications. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the hydroxyl group. Its structure suggests potential biological activity, making it of interest in medicinal chemistry and drug development. The bromine substituent can enhance the compound's lipophilicity and influence its interaction with biological targets. Additionally, the indazole framework is known for its presence in various pharmacologically active compounds, which may suggest that 7-bromo-1H-indazol-5-ol could serve as a scaffold for further chemical modifications aimed at optimizing its therapeutic properties. As with many heterocycles, it may also participate in various chemical reactions, including nucleophilic substitutions and coupling reactions, making it a versatile building block in organic synthesis.

7-bromo-1H-indazol-5-ol

1512720-83-0: 7-Bromo-1H-indazol-5-ol is a chemical compound characterized by its indazole core, which is a five-membered heterocyclic structure containing two nitrogen atoms. The presence of a bromine atom at the 7-position and a hydroxyl group (-OH) at the 5-position contributes to its unique reactivity and potential applications. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the hydroxyl group. Its structure suggests potential biological activity, making it of interest in medicinal chemistry and drug development. The bromine substituent can enhance the compound's lipophilicity and influence its interaction with biological targets. Additionally, the indazole framework is known for its presence in various pharmacologically active compounds, which may suggest that 7-bromo-1H-indazol-5-ol could serve as a scaffold for further chemical modifications aimed at optimizing its therapeutic properties. As with many heterocycles, it may also participate in various chemical reactions, including nucleophilic substitutions and coupling reactions, making it a versatile building block in organic synthesis.

CAS 1512720-83-0

7-bromo-1H-indazol-5-ol

1H-Indazol-5-ol, 7-bromo-

Ref: IN-DA001N7R

7-Bromo-1H-indazol-5-ol

Ref: 54-OR77861

7-BROMO-1H-INDAZOL-5-OL

Ref: 10-F858911