5-(Difluoromethoxy)-2-mercapto-1H-benzimidazole CAS: 97963-62-7
Catalog Number | XD93934 |
Product Name | 5-(Difluoromethoxy)-2-mercapto-1H-benzimidazole |
CAS | 97963-62-7 |
Molecular Formula | C8H6F2N2OS |
Molecular Weight | 216.21 |
Storage Details | Ambient |
Product Specification
Appearance | White powder |
Assay | 99% min |
5-(Difluoromethoxy)-2-mercapto-1H-benzimidazole is a chemical compound with the molecular formula C8H6F2N2OS. It is commonly referred to as DFB or difluoromethoxybenzimidazole. This compound has various applications in different fields due to its unique properties.One of the primary uses of 5-(Difluoromethoxy)-2-mercapto-1H-benzimidazole is as a pharmaceutical intermediate. It serves as a building block in the synthesis of drugs, particularly in the development of antiviral and anticancer agents. The presence of both a benzimidazole ring and a difluoromethoxy group in DFB makes it a valuable precursor for the creation of new therapeutic compounds with enhanced bioactivity and improved pharmacological properties.The difluoromethoxy group in 5-(Difluoromethoxy)-2-mercapto-1H-benzimidazole also imparts desirable physicochemical properties to the compound. It enhances lipophilicity, which is crucial for drug absorption and distribution in the body. This property makes DFB an attractive candidate for drug discovery and formulation, as it can potentially improve the bioavailability and therapeutic efficacy of pharmaceutical compounds.Furthermore, 5-(Difluoromethoxy)-2-mercapto-1H-benzimidazole exhibits antimicrobial activity. This characteristic has led to its use as an active ingredient in the development of antifungal and antibacterial agents. The compound's mechanism of action involves interfering with essential cellular processes of microorganisms, making it effective against a variety of harmful pathogens. This makes DFB a promising candidate for combating drug-resistant microbial strains and addressing the growing problem of antimicrobial resistance.In addition to pharmaceutical applications, 5-(Difluoromethoxy)-2-mercapto-1H-benzimidazole is used in academic research and chemical synthesis. Its unique structural features and reactivity make it valuable for studying and modifying the properties of benzimidazole derivatives. Researchers rely on DFB to introduce specific functional groups or create new compounds with desired properties during their investigations.It is important to handle 5-(Difluoromethoxy)-2-mercapto-1H-benzimidazole with caution, as it is a potent and potentially hazardous compound. Proper safety protocols, including the use of personal protective equipment and adherence to established laboratory practices, should be followed when working with this chemical.In summary, 5-(Difluoromethoxy)-2-mercapto-1H-benzimidazole is a versatile compound with applications in pharmaceuticals, antimicrobial agents, and chemical synthesis. Its unique structural features and reactivity make it valuable for drug development, particularly for antiviral and anticancer drugs. The compound's antimicrobial properties also make it useful for addressing drug-resistant pathogens. Responsible handling and adherence to safety measures are crucial when working with this compound.