4H-Indeno[1,2-b]thiophen-4-one is an organic compound characterized by its fused ring structure, which includes an indene and a thiophene moiety. This compound features a carbonyl group (ketone) at the 4-position of the indeno ring system, contributing to its reactivity and potential applications in organic synthesis and materials science. It is typically a solid at room temperature and exhibits a distinct aromatic character due to the presence of conjugated double bonds within its structure. The compound is of interest in various fields, including organic electronics, as it may possess semiconducting properties. Additionally, its unique structure allows for potential applications in dye-sensitized solar cells and organic light-emitting diodes (OLEDs). The compound's solubility and stability can vary depending on the solvent and environmental conditions, making it important to consider these factors in practical applications. Safety data should be reviewed before handling, as with any chemical substance, to ensure proper precautions are taken.

4H-Indeno[1,2-b]thiophen-4-one

Find at CymitQuimica all products linked to CAS 5706-08-1. Enter now to get more information

4H-Indeno[1,2-b]thiophen-4-one is a hydrolyzed carboxyl group that is used in the production of thionyl chloride and malonitrile. It is also known as a sensitizer for photoconductive and electrophotographic materials. 4H-Indeno[1,2-b]thiophen-4-one is used as a monomer for the synthesis of polymers, such as polycarbonates and polyurethanes. This compound has been shown to be an effective sensitizer for photopolymerization when combined with benzoyl chloride or benzoic acid. 4H-Indeno[1,2-b]thiophen-4-one can be used as a dehydrating agent in organic synthesis reactions that require removal of water from the reaction mixture.

CAS 5706-08-1: 4H-Indeno[1,2-b]thiophen-4-one

4H-Indeno[1,2-b]thiophen-4-one

Ref: 3B-I1003

4H-Indeno[1,2-b]thiophen-4-one

Ref: IN-DA00EGLB

4H-Indeno[1,2-b]thiophen-4-one

Ref: 3D-FAA70608