CAS 153483-31-9

2H-Cyclohepta[b]furan-2-one,6-[1-(acetyloxy)-3-oxobutyl]-3,3a,4,7,8,8a-hexahydro-7-methyl-3-methylene-,[3aR-[3aa,6(S*),7b,8ab]]- (9CI)

Description:

2H-Cyclohepta[b]furan-2-one, 6-[1-(acetyloxy)-3-oxobutyl]-3,3a,4,7,8,8a-hexahydro-7-methyl-3-methylene-, is a complex organic compound characterized by its unique bicyclic structure, which includes a furan ring fused to a cycloheptane framework. The presence of multiple functional groups, such as an acetyloxy group and a ketone, contributes to its reactivity and potential applications in organic synthesis. This compound is likely to exhibit moderate to high lipophilicity due to its hydrophobic cyclic structure, which may influence its solubility in organic solvents. Additionally, the stereochemistry indicated by the specific notation suggests the presence of chiral centers, which could lead to enantiomeric forms with distinct biological activities. The compound's molecular complexity may also suggest potential uses in medicinal chemistry or as a precursor in the synthesis of more complex molecules. However, specific properties such as melting point, boiling point, and spectral data would require experimental determination or literature reference for precise characterization.

Formula: C₁₇H₂₂O₅

Xanthinin

CAS: 153483-31-9

Formula: C₁₇H₂₂O₅

Purity: 95%~99%

Color and Shape: Powder

Molecular weight: 306.358

Ref: BP-SBP00661

Xanthinin

CAS: 153483-31-9

Xanthinin is a xanthine derivative, which is synthesized from purine alkaloids. As a derivative, it shares a structural relationship with naturally occurring compounds found in various plant species. The mode of action of xanthine derivatives typically involves inhibition of phosphodiesterase enzymes, leading to an increase in cyclic AMP levels within cells, which influences several physiological processes, including smooth muscle relaxation and modulation of metabolic pathways.

Formula: C₁₇H₂₂O₅

Purity: Min. 95%

Molecular weight: 306.4 g/mol

Ref: 3D-DGA48331