4-(1H-Imidazol-4-yl)benzoic acid, with the CAS number 13569-97-6, is an organic compound characterized by the presence of both an imidazole and a carboxylic acid functional group. This compound features a benzoic acid moiety, where a 1H-imidazole ring is substituted at the para position. It is typically a white to off-white solid that is soluble in polar solvents such as water and alcohols, owing to the presence of the carboxylic acid group. The imidazole ring contributes to its potential biological activity, making it of interest in pharmaceutical research, particularly in the development of drugs targeting various biological pathways. The compound may exhibit properties such as antimicrobial or antifungal activity, and its derivatives are often explored for their roles in coordination chemistry and as ligands in metal complexes. Additionally, it can participate in various chemical reactions, including esterification and amidation, making it a versatile building block in organic synthesis.

4-(1H-IMIDAZOL-4-YL)BENZOIC ACID

13569-97-6: 4-(1H-Imidazol-4-yl)benzoic acid 95%, 4-(1H-Imidazol-5-yl)benzoic acid

4-(1H-Imidazol-4-yl)benzoic Acid

4-(1H-Imidazol-4-yl)benzoic acid

4-(1H-Imidazol-4-yl)benzoic acid is a white crystalline solid that is soluble in water. It is a coordination compound with two carboxylate functional groups and two imidazolyl ligands in the form of linear chains. The temperature of the reaction determines whether copper or nickel will be used as the metal ion. With copper, 4-(1H-imidazol-4-yl)benzoic acid forms a mononuclear complex, whereas with nickel it forms a bidentate complex. This chemical has been shown to have antimicrobial activity against bacteria and fungi, including methicillin resistant Staphylococcus aureus (MRSA).

CAS 13569-97-6: 4-(1H-IMIDAZOL-4-YL)BENZOIC ACID

4-(1H-Imidazol-4-yl)benzoic Acid

Ref: 10-F065841

4-(1H-Imidazol-4-yl)benzoic acid

Ref: 54-OR6239

4-(1H-Imidazol-4-yl)benzoic acid

Ref: 3D-NAA56997

4-(1H-IMIDAZOL-4-YL)BENZOIC ACID

Ref: IN-DA0072JC