5-Fluoro-2,3-thiophenedicarboxaldehyde is an organic compound characterized by the presence of a thiophene ring, which is a five-membered aromatic heterocycle containing sulfur. This compound features two aldehyde functional groups (-CHO) and a fluorine atom substituted at the 5-position of the thiophene ring. The presence of the aldehyde groups contributes to its reactivity, making it useful in various synthetic applications, including the preparation of more complex organic molecules. The fluorine atom can influence the electronic properties of the compound, potentially enhancing its reactivity and solubility in certain solvents. Additionally, the thiophene moiety can impart unique properties such as increased stability and the ability to participate in π-π stacking interactions. This compound may find applications in pharmaceuticals, agrochemicals, or materials science due to its distinctive structural features and reactivity. As with many organic compounds, handling should be done with care, considering potential toxicity and environmental impact.

5-fluoro-2,3-thiophenedicarboxaldehyde

1015071-22-3: 5-Fluoro-2,3-thiophenedicarboxaldehyde is an organic compound characterized by the presence of a thiophene ring, which is a five-membered aromatic heterocycle containing sulfur. This compound features two aldehyde functional groups (-CHO) and a fluorine atom substituted at the 5-position of the thiophene ring. The presence of the aldehyde groups contributes to its reactivity, making it useful in various synthetic applications, including the preparation of more complex organic molecules. The fluorine atom can influence the electronic properties of the compound, potentially enhancing its reactivity and solubility in certain solvents. Additionally, the thiophene moiety can impart unique properties such as increased stability and the ability to participate in π-π stacking interactions. This compound may find applications in pharmaceuticals, agrochemicals, or materials science due to its distinctive structural features and reactivity. As with many organic compounds, handling should be done with care, considering potential toxicity and environmental impact.

CAS 1015071-22-3

5-fluoro-2,3-thiophenedicarboxaldehyde

5-Fluoro-2,3-Thiophenedicarboxaldehyde

Ref: IN-DA0004O4