2,4-Thiophenedicarboxaldehyde, with the CAS number 932-93-4, is an organic compound characterized by its thiophene ring structure, which is a five-membered aromatic heterocycle containing sulfur. This compound features two aldehyde functional groups (-CHO) located at the 2 and 4 positions of the thiophene ring, making it a dicarboxaldehyde. It is typically a yellow to brown solid at room temperature and is soluble in organic solvents such as ethanol and dichloromethane. The presence of the aldehyde groups contributes to its reactivity, allowing it to participate in various chemical reactions, including condensation and polymerization. 2,4-Thiophenedicarboxaldehyde is of interest in organic synthesis and materials science, particularly in the development of conductive polymers and organic semiconductors. Additionally, its unique structure may impart interesting optical and electronic properties, making it a subject of research in fields such as organic electronics and photonics. Safety precautions should be taken when handling this compound, as it may pose health risks if inhaled or ingested.

2,4-Thiophenedicarboxaldehyde

932-93-4: 2,4-Thiophenedicarboxaldehyde, with the CAS number 932-93-4, is an organic compound characterized by its thiophene ring structure, which is a five-membered aromatic heterocycle containing sulfur. This compound features two aldehyde functional groups (-CHO) located at the 2 and 4 positions of the thiophene ring, making it a dicarboxaldehyde. It is typically a yellow to brown solid at room temperature and is soluble in organic solvents such as ethanol and dichloromethane. The presence of the aldehyde groups contributes to its reactivity, allowing it to participate in various chemical reactions, including condensation and polymerization. 2,4-Thiophenedicarboxaldehyde is of interest in organic synthesis and materials science, particularly in the development of conductive polymers and organic semiconductors. Additionally, its unique structure may impart interesting optical and electronic properties, making it a subject of research in fields such as organic electronics and photonics. Safety precautions should be taken when handling this compound, as it may pose health risks if inhaled or ingested.

CAS 932-93-4

2,4-Thiophenedicarboxaldehyde

Thiophene-2,4-dicarbaldehyde

Ref: IN-DA00H2AI

Thiophene-2,4-dicarboxaldehyde

Ref: 54-OR13258

Thiophene-2,4-dicarbaldehyde

Ref: 10-F695117