CAS 1007882-27-0
:4,4'-Bis(2-((S)-pyrrolidin-2-yl)-1H-imidazol-5-yl)-1,1'-biphenyl
Description:
4,4'-Bis(2-((S)-pyrrolidin-2-yl)-1H-imidazol-5-yl)-1,1'-biphenyl is a complex organic compound characterized by its biphenyl backbone, which is substituted with imidazole and pyrrolidine groups. This compound features two imidazole rings, each linked to a pyrrolidine moiety, contributing to its potential biological activity and interaction with various biological targets. The presence of the chiral (S)-pyrrolidine indicates that the compound may exhibit stereospecific properties, which can influence its pharmacological effects. The imidazole rings are known for their role in coordination chemistry and biological systems, often participating in hydrogen bonding and metal coordination. This compound may be of interest in medicinal chemistry, particularly in the development of pharmaceuticals, due to its structural complexity and potential for specific interactions with biological macromolecules. Its solubility, stability, and reactivity would depend on the specific conditions and solvents used, making it essential to consider these factors in practical applications.
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Found 2 products.
4,4'-Bis(2-((S)-pyrrolidin-2-yl)-1H-imidazol-5-yl)-1,1'-biphenyl
CAS:Formula:C26H28N6Molecular weight:424.54074,4'-Bis(2-((S)-pyrrolidin-2-yl)-1H-imidazol-5-yl)-1,1'-biphenyl
CAS:<p>4,4'-Bis(2-((S)-pyrrolidin-2-yl)-1H-imidazol-5-yl)-1,1'-biphenyl is a drug product that has been custom synthesized to meet the needs of specific research and development. The CAS number for this compound is 1007882-27-0. It has a purity of ≥99%. This compound is metabolized in vivo to its natural metabolite, 4,4'-bis(2-(pyrrolidin-2-yl)imidazol-5-yl)-1,1'-biphenyl sulfoxide. Metabolism studies have been conducted on rats.</p>Formula:C26H28N6Purity:Min. 95%Molecular weight:424.5 g/mol
