CAS 89475-33-2

[1,2'-Binaphthalene]-5,5',8,8'-tetrone, 1',4-dihydroxy-2,3'-dimethyl-

Description:

[1,2'-Binaphthalene]-5,5',8,8'-tetrone, 1',4-dihydroxy-2,3'-dimethyl- is a complex organic compound characterized by its polycyclic structure, which consists of two naphthalene units connected by a tetrone moiety. This compound features multiple functional groups, including hydroxyl (-OH) groups and carbonyl (C=O) groups, contributing to its reactivity and potential applications in organic synthesis and materials science. The presence of methyl groups enhances its solubility and may influence its electronic properties. As a derivative of binaphthalene, it exhibits chirality, which can be significant in stereochemical applications. The compound's unique structure may also impart interesting optical properties, making it a candidate for studies in photochemistry and photophysics. Additionally, its CAS number, 89475-33-2, allows for easy identification in chemical databases. Overall, this substance is of interest in various fields, including organic chemistry, medicinal chemistry, and materials science, due to its distinctive characteristics and potential utility in research and development.

Formula: C₂₂H₁₄O₆

[1,2'-Binaphthalene]-5,5',8,8'-tetrone, 1',4-dihydroxy-2,3'-dimethyl-

CAS: 89475-33-2

Formula: C₂₂H₁₄O₆

Molecular weight: 374.343

Ref: IN-DA0043D0

rac-Isodiospyrin

Controlled Product

CAS: 89475-33-2

Formula: C₂₂H₁₄O₆

Color and Shape: Neat

Molecular weight: 327.33

Ref: TR-I815075

rac-Isodiospyrin

CAS: 89475-33-2

Isodiospyrin is a synthetic compound that is used in the synthesis of other compounds. It has been shown to inhibit cell growth in a number of different types of cells, including human leukemia cells and colon cancer cells. Isodiospyrin has also been shown to have potent inhibitory activity against the fatty acid synthase enzyme and the redox potentials it generates. This compound was found to be synthesized from two natural compounds, namely the plant families, quinone and dihydrobenzoquinone. The synthesis process involves an aldol cyclization reaction between these two compounds.

Formula: C₂₂H₁₄O₆

Purity: Min. 95%

Molecular weight: 374.3 g/mol

Ref: 3D-PDA47533