2-(2-Thienyl)furan is an organic compound characterized by the presence of both a furan and a thiophene ring in its structure. It features a furan ring, which is a five-membered aromatic heterocycle containing one oxygen atom, and a thiophene ring, which is a five-membered aromatic heterocycle containing one sulfur atom. This compound is typically a yellow to brown liquid or solid, depending on its purity and form. It is known for its potential applications in organic synthesis and materials science, particularly in the development of electronic materials and as a building block in the synthesis of more complex organic molecules. The presence of both sulfur and oxygen in its structure can impart unique electronic properties, making it of interest in various chemical and pharmaceutical research fields. Additionally, 2-(2-Thienyl)furan may exhibit interesting reactivity patterns due to the electron-rich nature of the thiophene and furan rings, which can participate in various chemical reactions such as electrophilic substitutions and polymerizations.

2-(2-Thienyl)furan

27521-80-8: 2-(2-Thienyl)furan is an organic compound characterized by the presence of both a furan and a thiophene ring in its structure. It features a furan ring, which is a five-membered aromatic heterocycle containing one oxygen atom, and a thiophene ring, which is a five-membered aromatic heterocycle containing one sulfur atom. This compound is typically a yellow to brown liquid or solid, depending on its purity and form. It is known for its potential applications in organic synthesis and materials science, particularly in the development of electronic materials and as a building block in the synthesis of more complex organic molecules. The presence of both sulfur and oxygen in its structure can impart unique electronic properties, making it of interest in various chemical and pharmaceutical research fields. Additionally, 2-(2-Thienyl)furan may exhibit interesting reactivity patterns due to the electron-rich nature of the thiophene and furan rings, which can participate in various chemical reactions such as electrophilic substitutions and polymerizations.

CAS 27521-80-8

2-(2-Thienyl)furan

2-(Thiophen-2-yl)furan

Ref: IN-DA002U0D