2,6-Dibromo-4,8-bis[(2-butyloctyl)oxy]thieno[2,3-f][1]benzothiophene(CAS: 1336893-15-2)

2,6-Dibromo-4,8-bis[(2-butyloctyl)oxy]thieno[2,3-f][1]benzothiophene is a solid with a crystalline form. Its molecular weight is approximately 614.38 g/mol. The compound is sparingly soluble in common organic solvents. It is not highly reactive under normal conditions but can undergo bromination and oxidation reactions. It has a high boiling point and low vapor pressure.

2,6-Dibromo-4,8-bis[(2-butyloctyl)oxy]thieno[2,3-f][1]benzothiophene is synthesized through a multistep process involving bromination of a thieno[2,3-f][1]benzothiophene derivative followed by alkoxylation using 2-butyloctanol. Commonly used catalysts include sulfuric acid and potassium bromide. The synthetic yield is around 70-80%, and the reaction is typically carried out under mild conditions to ensure selectivity.

2,6-Dibromo-4,8-bis[(2-butyloctyl)oxy]thieno[2,3-f][1]benzothiophene is used in the pharmaceutical industry for the development of certain drug candidates. It is also utilized in the polymer industry for enhancing the properties of certain materials. Additionally, it has potential applications in semiconductors and organic electronics due to its unique chemical structure and electronic properties.

Proper handling of 2,6-Dibromo-4,8-bis[(2-butyloctyl)oxy]thieno[2,3-f][1]benzothiophene requires the use of personal protective equipment (PPE) such as gloves, goggles, and a lab coat. Work should be conducted in a well-ventilated area or under a fume hood to minimize exposure. Spills should be cleaned up carefully, and the material should be disposed of according to local regulations. It is important to have a safety data sheet (SDS) readily available for reference.