Tert-butyl [(1S,2S,4R,6E)-4-({(1S,2S)-1-[(1H-benzimidazol-2-ylmethyl)carbamoyl]-2-methylbutyl}carbamoyl)-1-benzyl-2-hydroxy-7-phenylhept-6-en-1-yl]carbamate, with CAS number 132565-33-4, is a complex organic compound characterized by its intricate molecular structure, which includes multiple functional groups such as carbamates and hydroxyl groups. This compound features a tert-butyl group, which contributes to its hydrophobic characteristics, enhancing its solubility in organic solvents. The presence of a benzimidazole moiety suggests potential biological activity, as benzimidazole derivatives are often associated with pharmacological properties. The stereochemistry indicated by the (1S,2S,4R) and (6E) descriptors implies specific spatial arrangements that can influence the compound's reactivity and interactions with biological targets. Additionally, the compound's heptene backbone and various substituents may affect its stability and reactivity, making it a subject of interest in medicinal chemistry and drug design. Overall, this compound exemplifies the complexity and diversity of organic molecules used in various chemical and pharmaceutical applications.

tert-butyl [(1S,2S,4R,6E)-4-({(1S,2S)-1-[(1H-benzimidazol-2-ylmethyl)carbamoyl]-2-methylbutyl}carbamoyl)-1-benzyl-2-hydroxy-7-phenylhept-6-en-1-yl]carbamate

132565-33-4: Tert-butyl [(1S,2S,4R,6E)-4-({(1S,2S)-1-[(1H-benzimidazol-2-ylmethyl)carbamoyl]-2-methylbutyl}carbamoyl)-1-benzyl-2-hydroxy-7-phenylhept-6-en-1-yl]carbamate, with CAS number 132565-33-4, is a complex organic compound characterized by its intricate molecular structure, which includes multiple functional groups such as carbamates and hydroxyl groups. This compound features a tert-butyl group, which contributes to its hydrophobic characteristics, enhancing its solubility in organic solvents. The presence of a benzimidazole moiety suggests potential biological activity, as benzimidazole derivatives are often associated with pharmacological properties. The stereochemistry indicated by the (1S,2S,4R) and (6E) descriptors implies specific spatial arrangements that can influence the compound's reactivity and interactions with biological targets. Additionally, the compound's heptene backbone and various substituents may affect its stability and reactivity, making it a subject of interest in medicinal chemistry and drug design. Overall, this compound exemplifies the complexity and diversity of organic molecules used in various chemical and pharmaceutical applications.

L 687908 is a potent inhibitor of hydroxyethylene-containing HIV protease.

CAS 132565-33-4

tert-butyl [(1S,2S,4R,6E)-4-({(1S,2S)-1-[(1H-benzimidazol-2-ylmethyl)carbamoyl]-2-methylbutyl}carbamoyl)-1-benzyl-2-hydroxy-7-phenylhept-6-en-1-yl]carbamate

L 687908

Ref: TM-T24336