3-Phenoxythiophene-2-carbaldehyde is an organic compound characterized by its unique structure, which includes a thiophene ring, a phenoxy group, and an aldehyde functional group. The presence of the thiophene ring imparts aromatic properties, while the phenoxy group enhances its reactivity and solubility in organic solvents. This compound typically exhibits a pale yellow to light brown appearance and is soluble in various organic solvents such as dichloromethane and ethanol. Its aldehyde functionality makes it susceptible to oxidation and nucleophilic attack, which can be exploited in synthetic organic chemistry for further transformations. Additionally, 3-phenoxythiophene-2-carbaldehyde may exhibit interesting photophysical properties, making it a candidate for applications in organic electronics and materials science. Due to its structural features, it may also participate in various chemical reactions, including condensation and polymerization, contributing to its utility in the development of novel materials and pharmaceuticals. Safety data should be consulted for handling and storage, as with any chemical substance.

3-PHENOXYTHIOPHENE-2-CARBALDEHYDE

132706-25-3: 3-Phenoxythiophene-2-carbaldehyde is an organic compound characterized by its unique structure, which includes a thiophene ring, a phenoxy group, and an aldehyde functional group. The presence of the thiophene ring imparts aromatic properties, while the phenoxy group enhances its reactivity and solubility in organic solvents. This compound typically exhibits a pale yellow to light brown appearance and is soluble in various organic solvents such as dichloromethane and ethanol. Its aldehyde functionality makes it susceptible to oxidation and nucleophilic attack, which can be exploited in synthetic organic chemistry for further transformations. Additionally, 3-phenoxythiophene-2-carbaldehyde may exhibit interesting photophysical properties, making it a candidate for applications in organic electronics and materials science. Due to its structural features, it may also participate in various chemical reactions, including condensation and polymerization, contributing to its utility in the development of novel materials and pharmaceuticals. Safety data should be consulted for handling and storage, as with any chemical substance.

CAS 132706-25-3

3-PHENOXYTHIOPHENE-2-CARBALDEHYDE

3-Phenoxythiophene-2-carbaldehyde

Ref: IN-DA00110O

3-Phenoxythiophene-2-carboxaldehyde

Ref: 54-OR25439

3-Phenoxythiophene-2-carbaldehyde

Ref: 10-F635789