(4-Aminophenyl)(thiophen-2-yl)methanol is an organic compound characterized by the presence of both an amino group and a thiophene ring, which contribute to its chemical properties and potential applications. The compound features a phenolic structure due to the methanol moiety, which can participate in hydrogen bonding, enhancing its solubility in polar solvents. The amino group at the para position of the phenyl ring can act as a nucleophile, making the compound reactive in various chemical reactions, including electrophilic substitutions. The thiophene ring introduces aromaticity and can influence the electronic properties of the molecule, potentially affecting its reactivity and interaction with biological systems. This compound may exhibit interesting pharmacological properties, making it a candidate for further research in medicinal chemistry. Its unique structure allows for potential applications in organic synthesis, materials science, and as a building block in the development of novel pharmaceuticals. Overall, (4-aminophenyl)(thiophen-2-yl)methanol is a versatile compound with significant implications in various fields of chemistry.

(4-aminophenyl)(thiophen-2-yl)methanol

915919-62-9: (4-Aminophenyl)(thiophen-2-yl)methanol is an organic compound characterized by the presence of both an amino group and a thiophene ring, which contribute to its chemical properties and potential applications. The compound features a phenolic structure due to the methanol moiety, which can participate in hydrogen bonding, enhancing its solubility in polar solvents. The amino group at the para position of the phenyl ring can act as a nucleophile, making the compound reactive in various chemical reactions, including electrophilic substitutions. The thiophene ring introduces aromaticity and can influence the electronic properties of the molecule, potentially affecting its reactivity and interaction with biological systems. This compound may exhibit interesting pharmacological properties, making it a candidate for further research in medicinal chemistry. Its unique structure allows for potential applications in organic synthesis, materials science, and as a building block in the development of novel pharmaceuticals. Overall, (4-aminophenyl)(thiophen-2-yl)methanol is a versatile compound with significant implications in various fields of chemistry.

CAS 915919-62-9

(4-aminophenyl)(thiophen-2-yl)methanol

(4-aminophenyl)(2-thienyl)methanol

Ref: 10-F308295