The chemical substance with the name "(1R,3aS,7aR)-7a-methyl-1-[(2R)-6-methyl-6-triethylsilyloxyheptan-2-yl]-2,3,3a,5,6,7-hexahydro-1H-inden-4-one" and CAS number "1101133-55-4" is a complex organic compound characterized by its specific stereochemistry and functional groups. It features a hexahydroindene core, which is a bicyclic structure known for its stability and versatility in organic synthesis. The presence of a ketone functional group (indicated by the "4-one" in the name) suggests potential reactivity in various chemical transformations, such as nucleophilic additions. The triethylsilyloxy group enhances the compound's solubility and stability, making it suitable for various applications in organic chemistry and potentially in medicinal chemistry. The stereochemical descriptors (1R, 3aS, 7aR) indicate specific spatial arrangements of atoms, which can significantly influence the compound's biological activity and interactions. Overall, this compound exemplifies the complexity and diversity of organic molecules, particularly those with multiple chiral centers and functional groups.

(1R,3aS,7aR)-7a-methyl-1-[(2R)-6-methyl-6-triethylsilyloxyheptan-2-yl]-2,3,3a,5,6,7-hexahydro-1H-inden-4-one

1101133-55-4: The chemical substance with the name "(1R,3aS,7aR)-7a-methyl-1-[(2R)-6-methyl-6-triethylsilyloxyheptan-2-yl]-2,3,3a,5,6,7-hexahydro-1H-inden-4-one" and CAS number "1101133-55-4" is a complex organic compound characterized by its specific stereochemistry and functional groups. It features a hexahydroindene core, which is a bicyclic structure known for its stability and versatility in organic synthesis. The presence of a ketone functional group (indicated by the "4-one" in the name) suggests potential reactivity in various chemical transformations, such as nucleophilic additions. The triethylsilyloxy group enhances the compound's solubility and stability, making it suitable for various applications in organic chemistry and potentially in medicinal chemistry. The stereochemical descriptors (1R, 3aS, 7aR) indicate specific spatial arrangements of atoms, which can significantly influence the compound's biological activity and interactions. Overall, this compound exemplifies the complexity and diversity of organic molecules, particularly those with multiple chiral centers and functional groups.

CAS 1101133-55-4

(1R,3aS,7aR)-7a-methyl-1-[(2R)-6-methyl-6-triethylsilyloxyheptan-2-yl]-2,3,3a,5,6,7-hexahydro-1H-inden-4-one

Calcitriol Impurity 30

Ref: 4Z-C-129039

Calcitriol Impurity 30

Ref: ST-EA-CP-C49018