3-(5,6-Dimethyl-1H-benzimidazol-2-yl)propanoic acid, identified by its CAS number 173737-04-7, is an organic compound characterized by its benzimidazole core, which is a bicyclic structure containing both benzene and imidazole rings. This compound features a propanoic acid functional group, contributing to its acidic properties. The presence of two methyl groups at the 5 and 6 positions of the benzimidazole ring enhances its hydrophobic character and may influence its biological activity. Typically, compounds of this nature are studied for their potential pharmaceutical applications, particularly in areas such as anti-cancer or anti-inflammatory therapies, due to the biological significance of benzimidazole derivatives. The compound is likely to exhibit moderate solubility in organic solvents and varying solubility in water, depending on pH. Its molecular structure suggests potential interactions with biological targets, making it a subject of interest in medicinal chemistry. As with many organic acids, it may also participate in acid-base reactions, influencing its behavior in different chemical environments.

3-(5,6-dimethyl-1H-benzimidazol-2-yl)propanoic acid

173737-04-7: 3-(5,6-Dimethyl-1H-benzimidazol-2-yl)propanoic acid, identified by its CAS number 173737-04-7, is an organic compound characterized by its benzimidazole core, which is a bicyclic structure containing both benzene and imidazole rings. This compound features a propanoic acid functional group, contributing to its acidic properties. The presence of two methyl groups at the 5 and 6 positions of the benzimidazole ring enhances its hydrophobic character and may influence its biological activity. Typically, compounds of this nature are studied for their potential pharmaceutical applications, particularly in areas such as anti-cancer or anti-inflammatory therapies, due to the biological significance of benzimidazole derivatives. The compound is likely to exhibit moderate solubility in organic solvents and varying solubility in water, depending on pH. Its molecular structure suggests potential interactions with biological targets, making it a subject of interest in medicinal chemistry. As with many organic acids, it may also participate in acid-base reactions, influencing its behavior in different chemical environments.

CAS 173737-04-7

3-(5,6-dimethyl-1H-benzimidazol-2-yl)propanoic acid

1H-Benzimidazole-2-propanoic acid, 5,6-dimethyl-

Ref: IN-DA001Z5F

3-(5,6-Dimethyl-1H-benzo[d]imidazol-2-yl)propanoic acid

Ref: 54-OR1064567

3-(5,6-Dimethyl-1H-benzoimidazol-2-yl)-propionic acid

Ref: 10-F058920