Thiophene, 4-methyl-2-phenyl- is an organic compound characterized by a five-membered aromatic ring containing sulfur, specifically a thiophene ring substituted with a methyl group and a phenyl group. This compound exhibits typical thiophene properties, including a planar structure that contributes to its aromaticity, which enhances its stability and reactivity. The presence of the methyl and phenyl substituents influences its electronic properties, making it more lipophilic and potentially reactive in electrophilic substitution reactions. It is generally soluble in organic solvents and may exhibit fluorescence. Thiophene derivatives are of interest in various fields, including organic electronics, materials science, and pharmaceuticals, due to their unique electronic properties and potential applications in conducting polymers and dyes. The compound's behavior in chemical reactions can be influenced by the steric and electronic effects of the substituents, making it a subject of study in synthetic organic chemistry. Safety data should be consulted for handling and usage, as with all chemical substances.

Thiophene, 4-methyl-2-phenyl-

14300-29-9: Thiophene, 4-methyl-2-phenyl- is an organic compound characterized by a five-membered aromatic ring containing sulfur, specifically a thiophene ring substituted with a methyl group and a phenyl group. This compound exhibits typical thiophene properties, including a planar structure that contributes to its aromaticity, which enhances its stability and reactivity. The presence of the methyl and phenyl substituents influences its electronic properties, making it more lipophilic and potentially reactive in electrophilic substitution reactions. It is generally soluble in organic solvents and may exhibit fluorescence. Thiophene derivatives are of interest in various fields, including organic electronics, materials science, and pharmaceuticals, due to their unique electronic properties and potential applications in conducting polymers and dyes. The compound's behavior in chemical reactions can be influenced by the steric and electronic effects of the substituents, making it a subject of study in synthetic organic chemistry. Safety data should be consulted for handling and usage, as with all chemical substances.

CAS 14300-29-9

Thiophene, 4-methyl-2-phenyl-

4-methyl-2-phenylthiophene

Ref: 54-OR22160