Ethyl 5-cyano-3,4-dimethylthieno[2,3-b]thiophene-2-carboxylate is an organic compound characterized by its complex structure, which includes a thieno[2,3-b]thiophene core, a cyano group, and an ethyl ester functional group. This compound typically exhibits properties associated with heterocyclic compounds, such as potential electron-rich characteristics due to the presence of sulfur and nitrogen atoms in its structure. It is likely to be a solid at room temperature, with moderate solubility in organic solvents, reflecting its hydrophobic nature. The cyano group contributes to its reactivity, making it a potential candidate for various chemical reactions, including nucleophilic additions and cycloadditions. Additionally, the presence of multiple methyl groups can influence its steric properties and overall stability. This compound may find applications in organic electronics, particularly in the development of organic semiconductors or photovoltaic materials, due to its conjugated system that can facilitate charge transport. As with many organic compounds, safety precautions should be observed when handling it, given the potential toxicity associated with cyano-containing compounds.

ethyl 5-cyano-3,4-dimethylthieno[2,3-b]thiophene-2-carboxylate

175202-57-0: Ethyl 5-cyano-3,4-dimethylthieno[2,3-b]thiophene-2-carboxylate is an organic compound characterized by its complex structure, which includes a thieno[2,3-b]thiophene core, a cyano group, and an ethyl ester functional group. This compound typically exhibits properties associated with heterocyclic compounds, such as potential electron-rich characteristics due to the presence of sulfur and nitrogen atoms in its structure. It is likely to be a solid at room temperature, with moderate solubility in organic solvents, reflecting its hydrophobic nature. The cyano group contributes to its reactivity, making it a potential candidate for various chemical reactions, including nucleophilic additions and cycloadditions. Additionally, the presence of multiple methyl groups can influence its steric properties and overall stability. This compound may find applications in organic electronics, particularly in the development of organic semiconductors or photovoltaic materials, due to its conjugated system that can facilitate charge transport. As with many organic compounds, safety precautions should be observed when handling it, given the potential toxicity associated with cyano-containing compounds.

CAS 175202-57-0

ethyl 5-cyano-3,4-dimethylthieno[2,3-b]thiophene-2-carboxylate

Thieno[2,3-b]thiophene-2-carboxylic acid, 5-cyano-3,4-dimethyl-, ethyl ester

Ref: IN-DA0020H5

ethyl 5-cyano-3,4-dimethylthieno[2,3-b]thiophene-2-carboxylate

Ref: 54-OR25292