(2,5-Dimethyl-3-thienyl)phenylmethanone, with the CAS number 15271-04-2, is an organic compound characterized by its unique structure that includes a thienyl group and a phenylmethanone moiety. This compound features a thieno ring, which contributes to its aromatic properties and potential reactivity. The presence of two methyl groups at the 2 and 5 positions of the thienyl ring enhances its steric bulk and may influence its electronic properties, making it an interesting candidate for various chemical applications. The carbonyl group in the phenylmethanone part of the molecule is known for its reactivity in nucleophilic addition reactions, which can be exploited in synthetic chemistry. Additionally, the compound may exhibit interesting photophysical properties due to its conjugated system, making it potentially useful in materials science, particularly in organic electronics or as a dye. Its solubility and stability in different solvents can vary, which is important for its application in various chemical processes. Overall, this compound's structural features suggest a range of potential applications in organic synthesis and materials development.

(2,5-Dimethyl-3-thienyl)phenylmethanone

15271-04-2: Methanone, (2,5-dimethyl-3-thienyl)phenyl-, Ketone, 2,5-dimethyl-3-thienyl phenyl, 2,5-Dimethyl-3-benzoylthiophene, (2,5-Dimethyl-3-thienyl)phenylmethanone, (2,5-Dimethyl-thiophen-3-yl)-phenyl-methanone

(2,5-dimethylthiophen-3-yl)(phenyl)methanone

Methanone, (2,5-dimethyl-3-thienyl)phenyl-

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CAS 15271-04-2: (2,5-Dimethyl-3-thienyl)phenylmethanone

(2,5-dimethylthiophen-3-yl)(phenyl)methanone

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Methanone, (2,5-dimethyl-3-thienyl)phenyl-

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(2,5-dimethylthiophen-3-yl)(phenyl)methanone

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(2,5-Dimethylthiophen-3-yl)(phenyl)methanone

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