2-(2-Thienyl)phenol, with the CAS number 106584-13-8, is an organic compound characterized by the presence of both a phenolic hydroxyl group and a thienyl group. The thienyl moiety, derived from thiophene, contributes to the compound's aromatic properties and potential reactivity. This compound typically exhibits a solid state at room temperature and is soluble in organic solvents, reflecting its hydrophobic characteristics due to the aromatic systems. The presence of the hydroxyl group imparts some polar characteristics, allowing for hydrogen bonding, which can influence its solubility and reactivity in various chemical environments. 2-(2-Thienyl)phenol may exhibit interesting biological activities, making it a subject of interest in medicinal chemistry and materials science. Its structural features suggest potential applications in organic synthesis, as well as in the development of functional materials, due to the interplay between its aromatic and heteroaromatic components. Overall, this compound exemplifies the diverse chemistry associated with substituted phenols and heterocycles.

2-(2-thienyl) phenol

106584-13-8: 2-Thiophen-2-Ylphenol, 2-(Thiophen-2-Yl)Phenol

2-Thiophen-2-ylphenol

2 (2-THIENYL) PHENOL

2-(Thiophen-2-yl)phenol

2-(Thiophen-2-yl)phenol is an organic compound that has been synthesized in the laboratory. It is a member of the class of compounds called isocyanides, which are compounds that contain two or more cyanide groups. 2-(Thiophen-2-yl)phenol can be obtained via a palladium-catalyzed coupling reaction between thiophene and an isocyanide. The yield for this synthesis is 72%. This compound has shown to be useful for the introduction of functional groups into biomolecules with high yields, as well as being innovative in its use of synthetic methods.

CAS 106584-13-8: 2-(2-thienyl) phenol

2-Thiophen-2-ylphenol

Ref: 10-F608427

2 (2-THIENYL) PHENOL

Ref: IN-DA0083J1

2-(Thiophen-2-yl)phenol

Ref: 54-OR350383

2-(Thiophen-2-yl)phenol

Ref: 3D-GEA58413