CAS 14756-22-0

2-(4-methoxyphenyl)-4H-benzo[h]chromen-4-one

Description:

2-(4-Methoxyphenyl)-4H-benzo[h]chromen-4-one, also known by its CAS number 14756-22-0, is a synthetic organic compound characterized by its complex polycyclic structure, which includes a chromenone framework fused with a benzene ring. This compound typically exhibits properties associated with flavonoids, such as antioxidant activity, and may possess potential biological activities, including anti-inflammatory and anticancer effects. The presence of the methoxy group enhances its lipophilicity, potentially influencing its solubility and bioavailability. In terms of physical properties, it may appear as a crystalline solid, and its melting point and solubility can vary based on the specific conditions and purity. The compound's reactivity is influenced by the functional groups present, allowing for various chemical transformations. Its applications may extend to pharmaceuticals, agrochemicals, and materials science, where its unique structural features can be leveraged for specific functions. Overall, 2-(4-methoxyphenyl)-4H-benzo[h]chromen-4-one represents a significant compound of interest in both research and industrial contexts.

Formula: C₂₀H₁₄O₃

InChI: InChI=1/C20H14O3/c1-22-15-9-6-14(7-10-15)19-12-18(21)17-11-8-13-4-2-3-5-16(13)20(17)23-19/h2-12H,1H3

SMILES: COc1ccc(cc1)c1cc(=O)c2ccc3ccccc3c2o1

Synonyms:

• 14756-22-0
• 4H-Naphtho(1,2-b)pyran-4-one, 2-(4-methoxyphenyl)-
• 4'-Methoxy-7,8-benzoflavone
• 4'-Methoxy-a-naphthoflavone

4'-Methoxy-α-naphthoflavone

CAS: 14756-22-0

4'-Methoxy-alpha-naphthoflavone is a flavonoid that has been shown to have inhibitory effects on the metabolism of 3-methylcholanthrene and other xenobiotics. The compound inhibits the oxidation of these compounds by both the cytochrome P450 and NADPH-dependent oxidases. 4'-Methoxy-alpha-naphthoflavone also inhibits the activation of these compounds by hepatic tissues, as well as the metabolism of phenobarbital by rat liver microsomes. The compound may be metabolized in vivo to 4'-hydroxy-alpha-naphthoflavone, which is more potent than 4'-methoxy-alpha-naphthoflavone.

Formula: C₂₀H₁₄O₃

Purity: Min. 95%

Molecular weight: 302.32 g/mol

Ref: 3D-FM66350