1H-Benzimidazole-5,6-diol, also known by its CAS number 102169-73-3, is a heterocyclic organic compound characterized by its benzimidazole core structure, which consists of a fused benzene and imidazole ring. This compound features hydroxyl groups at the 5 and 6 positions of the benzimidazole ring, contributing to its chemical reactivity and potential biological activity. The presence of these hydroxyl groups enhances its solubility in polar solvents and may influence its interactions with biological targets. 1H-Benzimidazole-5,6-diol is of interest in medicinal chemistry due to its potential pharmacological properties, including antimicrobial and antifungal activities. Its structural features allow for various modifications, which can lead to the development of derivatives with enhanced efficacy or selectivity. Additionally, the compound may participate in hydrogen bonding and other intermolecular interactions, making it a valuable candidate for further research in drug development and material science. Overall, 1H-Benzimidazole-5,6-diol represents a significant compound in the study of heterocyclic chemistry and its applications in various fields.

1H-Benzimidazole-5,6-diol(9CI)

102169-73-3: 1H-Benzimidazole-5,6-diol, also known by its CAS number 102169-73-3, is a heterocyclic organic compound characterized by its benzimidazole core structure, which consists of a fused benzene and imidazole ring. This compound features hydroxyl groups at the 5 and 6 positions of the benzimidazole ring, contributing to its chemical reactivity and potential biological activity. The presence of these hydroxyl groups enhances its solubility in polar solvents and may influence its interactions with biological targets. 1H-Benzimidazole-5,6-diol is of interest in medicinal chemistry due to its potential pharmacological properties, including antimicrobial and antifungal activities. Its structural features allow for various modifications, which can lead to the development of derivatives with enhanced efficacy or selectivity. Additionally, the compound may participate in hydrogen bonding and other intermolecular interactions, making it a valuable candidate for further research in drug development and material science. Overall, 1H-Benzimidazole-5,6-diol represents a significant compound in the study of heterocyclic chemistry and its applications in various fields.

CAS 102169-73-3

1H-Benzimidazole-5,6-diol(9CI)

1H-Benzo[d]imidazole-5,6-diol

Ref: IN-DA0006SJ