3,4-Dibutylthiophene is an organic compound belonging to the thiophene family, characterized by a five-membered aromatic ring containing sulfur. Its structure features two butyl groups attached to the 3 and 4 positions of the thiophene ring, which significantly influences its physical and chemical properties. This compound is typically a colorless to pale yellow liquid with a distinctive odor. It is relatively non-polar, which affects its solubility in various solvents, making it more soluble in organic solvents than in water. 3,4-Dibutylthiophene exhibits interesting electronic properties, making it a candidate for applications in organic electronics, such as organic semiconductors and photovoltaic devices. Additionally, its stability and reactivity can be influenced by the presence of the butyl substituents, which can enhance its performance in various chemical reactions. Safety data indicates that, like many organic compounds, it should be handled with care, as it may pose health risks if inhaled or ingested. Overall, 3,4-Dibutylthiophene is a valuable compound in the field of organic chemistry and materials science.

3,4-Dibutylthiophene

85932-61-2: 3,4-Dibutylthiophene is an organic compound belonging to the thiophene family, characterized by a five-membered aromatic ring containing sulfur. Its structure features two butyl groups attached to the 3 and 4 positions of the thiophene ring, which significantly influences its physical and chemical properties. This compound is typically a colorless to pale yellow liquid with a distinctive odor. It is relatively non-polar, which affects its solubility in various solvents, making it more soluble in organic solvents than in water. 3,4-Dibutylthiophene exhibits interesting electronic properties, making it a candidate for applications in organic electronics, such as organic semiconductors and photovoltaic devices. Additionally, its stability and reactivity can be influenced by the presence of the butyl substituents, which can enhance its performance in various chemical reactions. Safety data indicates that, like many organic compounds, it should be handled with care, as it may pose health risks if inhaled or ingested. Overall, 3,4-Dibutylthiophene is a valuable compound in the field of organic chemistry and materials science.

<p>3,4-Dibutylthiophene is a photophysical compound that has been shown to have a blue-violet color. It is soluble in organic solvents and reacts with sodium sulfide to form the dibutylthiophenesulfide. 3,4-Dibutylthiophenesulfides have been used as infrared light absorbers in optical properties. The cross-coupling of 3,4-dibutylthiophenesulfides with tetrakistriphenylphosphine has also been studied for its ability to produce polyunsaturated compounds. 3,4-Dibutylthiophene has been shown to be an effective bactericide against certain strains of bacteria when combined with sodium sulfide and an organic solvent. The bacterial strain tested was not disclosed. 3,4-Dibutylthiophene can also be copolymerized with fatty acids and monomers such as terminal alk</p>

CAS 85932-61-2

3,4-Dibutylthiophene

3,4-Dibutylthiophene

Ref: 3D-FD153212