Trans-4-(2-thienyl)-3-buten-2-one, with the CAS number 33603-63-3, is an organic compound characterized by its unique structure that includes a thienyl group and a conjugated double bond system. This compound features a butenone backbone, which contributes to its reactivity and potential applications in organic synthesis. The presence of the thienyl ring, a five-membered aromatic heterocycle containing sulfur, imparts distinct electronic properties, enhancing its ability to participate in various chemical reactions, such as electrophilic substitutions or nucleophilic additions. Trans-4-(2-thienyl)-3-buten-2-one is typically a yellow to brown liquid or solid, depending on its purity and specific conditions. It is soluble in organic solvents, making it useful in various chemical processes. Additionally, the compound may exhibit biological activity, which has drawn interest in medicinal chemistry and material science. Its stability and reactivity can be influenced by environmental factors such as temperature and pH, making it a subject of study in both synthetic and applied chemistry contexts.

trans-4-(2-thienyl)-3-buten-2-one

33603-63-3: Trans-4-(2-thienyl)-3-buten-2-one, with the CAS number 33603-63-3, is an organic compound characterized by its unique structure that includes a thienyl group and a conjugated double bond system. This compound features a butenone backbone, which contributes to its reactivity and potential applications in organic synthesis. The presence of the thienyl ring, a five-membered aromatic heterocycle containing sulfur, imparts distinct electronic properties, enhancing its ability to participate in various chemical reactions, such as electrophilic substitutions or nucleophilic additions. Trans-4-(2-thienyl)-3-buten-2-one is typically a yellow to brown liquid or solid, depending on its purity and specific conditions. It is soluble in organic solvents, making it useful in various chemical processes. Additionally, the compound may exhibit biological activity, which has drawn interest in medicinal chemistry and material science. Its stability and reactivity can be influenced by environmental factors such as temperature and pH, making it a subject of study in both synthetic and applied chemistry contexts.

CAS 33603-63-3

trans-4-(2-thienyl)-3-buten-2-one

trans-4-(2-Thienyl)-3-buten-2-one

Ref: IN-DA007DJA

trans-4-(2-Thienyl)-3-buten-2-one

Ref: 54-OR1043534

(E)-4-(Thiophen-2-yl)but-3-en-2-one

Ref: 10-F758598