1-(2,2'-Bithiophen-5-yl)methanamine, with the CAS number 4380-96-5, is an organic compound characterized by its bithiophene structure, which consists of two thiophene rings connected by a single bond. This compound features an amine functional group (-NH2) attached to a methylene bridge (-CH2-) that links to the bithiophene moiety. The presence of the bithiophene structure imparts notable electronic properties, making it of interest in organic electronics, particularly in organic semiconductors and photovoltaic applications. The compound is typically a solid at room temperature and may exhibit solubility in organic solvents due to its aromatic nature. Its properties, such as melting point, boiling point, and reactivity, can vary based on the specific conditions and purity of the sample. Additionally, the amine group can participate in various chemical reactions, including nucleophilic substitutions and coupling reactions, which are valuable in synthetic organic chemistry. Overall, this compound is significant in materials science and organic synthesis due to its unique structural and electronic characteristics.

1-(2,2'-bithiophen-5-yl)methanamine

4380-96-5: 1-(2,2'-Bithiophen-5-yl)methanamine, with the CAS number 4380-96-5, is an organic compound characterized by its bithiophene structure, which consists of two thiophene rings connected by a single bond. This compound features an amine functional group (-NH2) attached to a methylene bridge (-CH2-) that links to the bithiophene moiety. The presence of the bithiophene structure imparts notable electronic properties, making it of interest in organic electronics, particularly in organic semiconductors and photovoltaic applications. The compound is typically a solid at room temperature and may exhibit solubility in organic solvents due to its aromatic nature. Its properties, such as melting point, boiling point, and reactivity, can vary based on the specific conditions and purity of the sample. Additionally, the amine group can participate in various chemical reactions, including nucleophilic substitutions and coupling reactions, which are valuable in synthetic organic chemistry. Overall, this compound is significant in materials science and organic synthesis due to its unique structural and electronic characteristics.

CAS 4380-96-5

1-(2,2'-bithiophen-5-yl)methanamine

2,2'-Bithiophene-5-methylamine

Ref: IN-DA00D9VY

5-(Aminomethyl)-[2,2']-bithiophene

Ref: 54-OR23235