5-Chloro-4-iodo-2-methoxybenzoic acid is an aromatic carboxylic acid characterized by the presence of a benzoic acid core substituted with a chlorine atom at the 5-position, an iodine atom at the 4-position, and a methoxy group at the 2-position. This compound typically exhibits a solid state at room temperature and is soluble in organic solvents, while its solubility in water may be limited due to the hydrophobic nature of the aromatic ring and the substituents. The presence of halogens (chlorine and iodine) can influence its reactivity, making it a potential candidate for various chemical reactions, including nucleophilic substitutions and coupling reactions. The methoxy group can also participate in hydrogen bonding, affecting the compound's physical properties and reactivity. Additionally, this compound may exhibit biological activity, making it of interest in pharmaceutical research. Its molecular structure contributes to its unique chemical properties, which can be explored in various applications, including organic synthesis and medicinal chemistry.

5-chloro-4-iodo-2-methoxybenzoic acid

473264-13-0: 5-Chloro-4-iodo-2-methoxybenzoic acid is an aromatic carboxylic acid characterized by the presence of a benzoic acid core substituted with a chlorine atom at the 5-position, an iodine atom at the 4-position, and a methoxy group at the 2-position. This compound typically exhibits a solid state at room temperature and is soluble in organic solvents, while its solubility in water may be limited due to the hydrophobic nature of the aromatic ring and the substituents. The presence of halogens (chlorine and iodine) can influence its reactivity, making it a potential candidate for various chemical reactions, including nucleophilic substitutions and coupling reactions. The methoxy group can also participate in hydrogen bonding, affecting the compound's physical properties and reactivity. Additionally, this compound may exhibit biological activity, making it of interest in pharmaceutical research. Its molecular structure contributes to its unique chemical properties, which can be explored in various applications, including organic synthesis and medicinal chemistry.

CAS 473264-13-0

5-chloro-4-iodo-2-methoxybenzoic acid

5-Chloro-4-iodo-2-methoxybenzoic acid

Ref: 54-OR1032976

5-CHLORO-4-IODO-2-METHOXYBENZOIC ACID

Ref: 10-F828765