5-Bromo-3,4-dimethylthieno[2,3-b]thiophene-2-carboxaldehyde is a heterocyclic organic compound characterized by its unique structure, which includes a thiophene ring fused with a thieno moiety. This compound features a bromine substituent at the 5-position and two methyl groups at the 3 and 4 positions, contributing to its distinct chemical properties. The presence of the aldehyde functional group at the 2-position enhances its reactivity, making it useful in various synthetic applications, particularly in organic synthesis and materials science. The compound is likely to exhibit moderate solubility in organic solvents, and its reactivity can be influenced by the electron-withdrawing nature of the aldehyde and the electron-donating effects of the methyl groups. Additionally, the bromine atom can serve as a site for further functionalization, allowing for the development of more complex molecules. Overall, this compound is of interest in the fields of organic chemistry and materials development due to its potential applications in electronic materials and pharmaceuticals.

5-BROMO-3,4-DIMETHYLTHIENO[2,3-B]THIOPHENE-2-CARBOXALDEHYDE

175202-64-9: 5-Bromo-3,4-dimethylthieno[2,3-b]thiophene-2-carboxaldehyde is a heterocyclic organic compound characterized by its unique structure, which includes a thiophene ring fused with a thieno moiety. This compound features a bromine substituent at the 5-position and two methyl groups at the 3 and 4 positions, contributing to its distinct chemical properties. The presence of the aldehyde functional group at the 2-position enhances its reactivity, making it useful in various synthetic applications, particularly in organic synthesis and materials science. The compound is likely to exhibit moderate solubility in organic solvents, and its reactivity can be influenced by the electron-withdrawing nature of the aldehyde and the electron-donating effects of the methyl groups. Additionally, the bromine atom can serve as a site for further functionalization, allowing for the development of more complex molecules. Overall, this compound is of interest in the fields of organic chemistry and materials development due to its potential applications in electronic materials and pharmaceuticals.

Thieno[2,3-b]thiophene-2-carboxaldehyde, 5-bromo-3,4-dimethyl-

<p>5-Bromo-3,4-dimethylthieno[2,3-b]thiophene-2-carboxaldehyde</p>

CAS 175202-64-9

5-BROMO-3,4-DIMETHYLTHIENO[2,3-B]THIOPHENE-2-CARBOXALDEHYDE

Thieno[2,3-b]thiophene-2-carboxaldehyde, 5-bromo-3,4-dimethyl-

Ref: IN-DA0020GY

5-Bromo-3,4-dimethylthieno[2,3-b]thiophene-2-carboxaldehyde

Ref: 54-OR103624