CAS 35408-03-8

Bicyclo[3.1.1]hept-3-en-2-one, 6,6-dimethyl-, (1R)-

Description:

Bicyclo[3.1.1]hept-3-en-2-one, 6,6-dimethyl-, (1R)-, with CAS number 35408-03-8, is a bicyclic organic compound characterized by its unique structure that includes a bicycloheptene framework. This compound features a ketone functional group at the 2-position and two methyl groups at the 6-position, contributing to its distinct chemical properties. The (1R) designation indicates a specific stereochemistry at the chiral center, which can influence its reactivity and interactions in chemical reactions. Bicyclic compounds like this one often exhibit interesting reactivity due to ring strain and the presence of multiple functional groups. The compound may be of interest in organic synthesis and medicinal chemistry, particularly for its potential applications in the development of pharmaceuticals or as a building block in complex organic molecules. Its physical properties, such as boiling point, melting point, and solubility, would depend on the specific molecular interactions and the presence of functional groups.

Formula: C₉H₁₂O

(+)-Apoverbenone

CAS: 35408-03-8

Formula: C₉H₁₂O

Molecular weight: 136.19

Ref: 4Z-V-081002

(+)-Apoverbenone

CAS: 35408-03-8

(+)-Apoverbenone is a chiral synthetic organic compound, which is derived through the chemical manipulation of natural terpenoids, often produced in stereoisomer-specific reactions. Its structure is central to its function, allowing interaction with biological pathways, which can be complex and varied depending on the specific system.

Formula: C₉H₁₂O

Purity: Min. 95%

Molecular weight: 136.19 g/mol

Ref: 3D-KBA40803