Methyl 2-chloro-4-(1H-imidazol-1-yl)benzenecarboxylate, with the CAS number 952182-93-3, is a chemical compound characterized by its aromatic structure and the presence of both a chloro and an imidazole functional group. This compound features a methyl ester group, which contributes to its solubility in organic solvents and potential reactivity in various chemical reactions. The imidazole ring is known for its biological significance, often found in pharmaceuticals and biologically active compounds, suggesting potential applications in medicinal chemistry. The chlorine atom introduces electrophilic characteristics, making the compound suitable for further derivatization. Its molecular structure indicates that it may exhibit interesting properties such as antimicrobial or antifungal activity, typical of compounds containing imidazole. Additionally, the presence of the carboxylate group may enhance its reactivity in esterification or amidation reactions. Overall, this compound represents a versatile building block in organic synthesis and medicinal chemistry, with potential implications in drug development and agrochemical applications.

methyl 2-chloro-4-(1H-imidazol-1-yl)benzenecarboxylate

952182-93-3: Methyl 2-chloro-4-(1H-imidazol-1-yl)benzenecarboxylate, with the CAS number 952182-93-3, is a chemical compound characterized by its aromatic structure and the presence of both a chloro and an imidazole functional group. This compound features a methyl ester group, which contributes to its solubility in organic solvents and potential reactivity in various chemical reactions. The imidazole ring is known for its biological significance, often found in pharmaceuticals and biologically active compounds, suggesting potential applications in medicinal chemistry. The chlorine atom introduces electrophilic characteristics, making the compound suitable for further derivatization. Its molecular structure indicates that it may exhibit interesting properties such as antimicrobial or antifungal activity, typical of compounds containing imidazole. Additionally, the presence of the carboxylate group may enhance its reactivity in esterification or amidation reactions. Overall, this compound represents a versatile building block in organic synthesis and medicinal chemistry, with potential implications in drug development and agrochemical applications.

Methyl 2-chloro-4-(1H-imidazol-1-yl)benzoate

CAS 952182-93-3

methyl 2-chloro-4-(1H-imidazol-1-yl)benzenecarboxylate

Methyl 2-chloro-4-(1H-imidazol-1-yl)benzoate

Ref: 54-OR33452