4,5-Dihydro-2-(ethoxycarbonyl)naphtho(1,2-b)thiophene is a chemical compound characterized by its unique structure, which includes a naphthalene core fused with a thiophene ring. This compound features a dihydro group, indicating the presence of two hydrogen atoms that contribute to its saturation. The ethoxycarbonyl group introduces an ester functionality, enhancing its reactivity and solubility in organic solvents. Typically, compounds of this nature exhibit interesting electronic properties due to the conjugated system formed by the naphthalene and thiophene moieties, which can lead to applications in organic electronics, such as organic semiconductors or photovoltaic materials. Additionally, the presence of the ethoxycarbonyl group may impart specific biological activities, making it a candidate for further pharmacological studies. The compound's stability, solubility, and reactivity can be influenced by the substituents on the naphthalene and thiophene rings, which can be tailored for desired applications in synthetic chemistry or materials science.

4,5-DIHYDRO-2-(ETHOXYCARBONYL)NAPTHO(1,2-B)THIOPENE

19397-74-1: 4,5-Dihydro-2-(ethoxycarbonyl)naphtho(1,2-b)thiophene is a chemical compound characterized by its unique structure, which includes a naphthalene core fused with a thiophene ring. This compound features a dihydro group, indicating the presence of two hydrogen atoms that contribute to its saturation. The ethoxycarbonyl group introduces an ester functionality, enhancing its reactivity and solubility in organic solvents. Typically, compounds of this nature exhibit interesting electronic properties due to the conjugated system formed by the naphthalene and thiophene moieties, which can lead to applications in organic electronics, such as organic semiconductors or photovoltaic materials. Additionally, the presence of the ethoxycarbonyl group may impart specific biological activities, making it a candidate for further pharmacological studies. The compound's stability, solubility, and reactivity can be influenced by the substituents on the naphthalene and thiophene rings, which can be tailored for desired applications in synthetic chemistry or materials science.

4,5-Dihydro-2-(ethoxycarbonyl)naphtho(1,2-b)thiophene

<p>Ethyl 4,5-dihydronaphtho[1,2-b]thiophene-2-carboxylate</p>

CAS 19397-74-1

4,5-DIHYDRO-2-(ETHOXYCARBONYL)NAPTHO(1,2-B)THIOPENE

4,5-Dihydro-2-(ethoxycarbonyl)naphtho(1,2-b)thiophene

Ref: IN-DA00AT70

Ethyl 4,5-dihydronaphtho[1,2-b]thiophene-2-carboxylate

Ref: 54-OR1050220

ETHYL 4,5-DIHYDRONAPHTHO[1,2-B]THIOPHENE-2-CARBOXYLATE

Ref: 10-F470929