2-Thiophen-2-ylbenzaldehyde, with the CAS number 99902-07-5, is an organic compound characterized by the presence of both a thiophene ring and a benzaldehyde functional group. This compound features a thiophene moiety substituted at the 2-position with a benzaldehyde group, which contributes to its aromatic properties. It typically appears as a yellow to brown liquid or solid, depending on its purity and specific conditions. The compound is known for its potential applications in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals, due to the reactivity of the aldehyde group and the electron-rich nature of the thiophene ring. Its molecular structure allows for various chemical reactions, including electrophilic substitutions and condensation reactions. Additionally, 2-thiophen-2-ylbenzaldehyde may exhibit interesting photophysical properties, making it a candidate for studies in materials science and organic electronics. Safety data should be consulted for handling and storage, as with any chemical substance.

2-thiophen-2-ylbenzaldehyde

99902-07-5: 2-(2-Thienyl)benzaldehyde, 2-Thien-2-Ylbenzaldehyde, Benzaldehyde, 2-(2-thienyl)-

2-(Thien-2-yl)benzaldehyde

2-Thien-2-ylbenzaldehyde is a benzene derivative that is synthesised through the Suzuki coupling reaction. It is mainly used as a precursor to other compounds and can be used in the synthesis of oxirane and chlorides. 2-Thien-2-ylbenzaldehyde has been used as a reagent for the Friedel-Crafts reaction, which is useful for the synthesis of pyridine rings. This compound has also been shown to be an effective reagent for cross-coupling reactions with various halides.

CAS 99902-07-5: 2-thiophen-2-ylbenzaldehyde

2-(Thien-2-yl)benzaldehyde

Ref: 54-OR1392

2-Thien-2-ylbenzaldehyde

Ref: 3D-FT144318

2-(Thiophen-2-yl)benzaldehyde

Ref: IN-DA003VM8

2-Thiophen-2-yl-benzaldehyde

Ref: 10-F032294