2,5-Diethylthiophene is a heterocyclic organic compound characterized by a five-membered aromatic ring containing sulfur. It features two ethyl groups attached to the 2 and 5 positions of the thiophene ring, which contributes to its unique chemical properties. This compound is typically a colorless to pale yellow liquid with a distinct odor. It is soluble in organic solvents such as ethanol and ether but has limited solubility in water due to its hydrophobic nature. 2,5-Diethylthiophene exhibits moderate stability under standard conditions but can undergo various chemical reactions, including electrophilic substitution, due to the electron-rich nature of the thiophene ring. Its structure allows for potential applications in organic electronics, particularly in the development of conductive polymers and materials for organic light-emitting diodes (OLEDs). Additionally, it may serve as an intermediate in the synthesis of other organic compounds. Safety data should be consulted for handling and exposure guidelines, as with any chemical substance.

2,5-Diethylthiophene

5069-23-8: Thiophene, 2,5-Diethyl-, 2,5-Diethylthiophene

2,5-Diethylthiophene is a chemical compound that has antioxidant potential. It is reactive with hydrochloric acid and chloromethylation of the surface methodology to form 2,5-dichlorothiophene. The chloride ion has been shown to be the chemical nature of this compound. Mathematical modeling has shown that it can react with potassium phosphate in a flow system at a rate proportional to the number of molecules of 2,5-diethylthiophene present. This reaction produces n-hexane and 2,5-dichlorothiophene as reaction products. The depression activity of this chemical has been studied using an animal model system and found to be due to its ability to inhibit monoamine oxidase type A (MAO-A).

CAS 5069-23-8: 2,5-Diethylthiophene

2,5-Diethylthiophene

Ref: 3D-FD146972