3-Chloro-1H-indazole-6-carboxylic acid is a chemical compound characterized by its indazole core, which is a five-membered heterocyclic structure containing two nitrogen atoms. The presence of a carboxylic acid functional group (-COOH) at the 6-position contributes to its acidic properties, while the chlorine substituent at the 3-position introduces unique reactivity and influences its chemical behavior. This compound is typically a solid at room temperature and is soluble in polar solvents, which is common for carboxylic acids. Its structure allows for potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to the indazole moiety's biological activity. Additionally, the chlorine atom can enhance the compound's lipophilicity and may affect its interaction with biological targets. As with many heterocyclic compounds, 3-chloro-1H-indazole-6-carboxylic acid may exhibit interesting properties such as fluorescence or specific reactivity in organic synthesis, making it a subject of interest in both research and industrial applications.

3-Chloro 1H-indazole-6-carboxylic acid

1086391-21-0: 3-Chloro-1H-indazole-6-carboxylic acid is a chemical compound characterized by its indazole core, which is a five-membered heterocyclic structure containing two nitrogen atoms. The presence of a carboxylic acid functional group (-COOH) at the 6-position contributes to its acidic properties, while the chlorine substituent at the 3-position introduces unique reactivity and influences its chemical behavior. This compound is typically a solid at room temperature and is soluble in polar solvents, which is common for carboxylic acids. Its structure allows for potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to the indazole moiety's biological activity. Additionally, the chlorine atom can enhance the compound's lipophilicity and may affect its interaction with biological targets. As with many heterocyclic compounds, 3-chloro-1H-indazole-6-carboxylic acid may exhibit interesting properties such as fluorescence or specific reactivity in organic synthesis, making it a subject of interest in both research and industrial applications.

CAS 1086391-21-0

3-Chloro 1H-indazole-6-carboxylic acid

3-Chloro 1H-indazole-6-carboxylic acid

Ref: IN-DA00999T

3-CHLORO-1H-INDAZOLE-6-CARBOXYLIC ACID

Ref: 10-F816843