1H-Benzimidazole-5,6-diamine, with the CAS number 71209-21-7, is an organic compound characterized by its benzimidazole core structure, which consists of a fused benzene and imidazole ring. This compound features two amino groups (-NH2) located at the 5 and 6 positions of the benzimidazole ring, contributing to its reactivity and potential applications in various fields. It is typically a solid at room temperature and may exhibit properties such as solubility in polar solvents, depending on the specific conditions. The presence of amino groups allows for hydrogen bonding and can influence the compound's interaction with biological systems, making it of interest in medicinal chemistry and drug development. Additionally, 1H-Benzimidazole-5,6-diamine may exhibit properties such as fluorescence or photostability, which can be advantageous in certain applications. Its derivatives and analogs are often explored for their potential therapeutic effects, including antimicrobial and anticancer activities. As with many chemical substances, safety data should be consulted to understand handling and toxicity considerations.

1H-Benzimidazole-5,6-diamine

71209-21-7: Benzimidazole,5,6-diamino- (7CI), 5,6-Diaminobenzimidazole

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

1,3-Benzodiazole-5,6-diamine is an antimicrobial agent that belongs to the group of benzimidazoles and has antifungal activities. It can be used for the treatment of infections caused by bacteria or fungi. 1,3-Benzodiazole-5,6-diamine binds to DNA gyrase and topoisomerase IV and inhibits bacterial growth. This drug also inhibits the synthesis of proteins in fungi and has been shown to inhibit the production of ergosterol, which is a major component of fungal cell membranes.

CAS 71209-21-7: 1H-Benzimidazole-5,6-diamine

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

Ref: IN-DA00FQWT

1H-1,3-Benzodiazole-5,6-diamine

Ref: 3D-WCA20921

1H-Benzimidazole-5,6-diamine

Ref: 10-F607083

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

Ref: 54-OR350495