CAS 39193-85-6
:bis(3-methoxyphenyl)methanone
Description:
Bis(3-methoxyphenyl)methanone, with the CAS number 39193-85-6, is an organic compound characterized by its structure, which features two 3-methoxyphenyl groups attached to a central carbonyl group (ketone). This compound typically appears as a solid at room temperature and is soluble in organic solvents due to its hydrophobic aromatic rings. The presence of methoxy groups enhances its electron-donating properties, which can influence its reactivity and interactions with other chemical species. Bis(3-methoxyphenyl)methanone may exhibit interesting photophysical properties, making it of interest in fields such as organic electronics and materials science. Additionally, its structural features may contribute to potential applications in pharmaceuticals or as intermediates in organic synthesis. As with many organic compounds, safety precautions should be taken when handling it, including the use of appropriate personal protective equipment, as it may pose health risks if ingested or inhaled.
Formula:C15H14O3
InChI:InChI=1/C15H14O3/c1-17-13-7-3-5-11(9-13)15(16)12-6-4-8-14(10-12)18-2/h3-10H,1-2H3
SMILES:COc1cccc(c1)C(=O)c1cccc(c1)OC
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Found 2 products.
Bis(3-methoxyphenyl)methanone
CAS:<p>Bis(3-methoxyphenyl)methanone is a palladium catalyst that selectively activates olefins. It has been shown to be useful in the synthesis of dihydrobenzofurans and oxonium derivatives, which are used as pharmaceuticals. This compound also catalyzes the transformation of various functional groups, such as diazo, alkenes, and intramolecular aldol condensation. Bis(3-methoxyphenyl)methanone is used as a catalyst for the production of dibenzofuran compounds with high selectivity. The diastereoselectivity of this compound is due to its ability to activate substrates with electron-donating groups at positions ortho to the phenyl group.</p>Formula:C15H14O3Purity:Min. 95%Molecular weight:242.27 g/mol
