CAS 15875-54-4

1H-Indene-1,3(2H)-dione, 2-[(4-chlorophenyl)methylene]-

Description:

1H-Indene-1,3(2H)-dione, 2-[(4-chlorophenyl)methylene]- is an organic compound characterized by its indene structure fused with a diketone functionality. This compound features a methylene bridge connecting a 4-chlorobenzyl group to the indene moiety, which contributes to its unique chemical properties. It typically exhibits a yellow to orange color in solid form and is soluble in organic solvents. The presence of the chlorophenyl group enhances its reactivity and may influence its biological activity, making it of interest in medicinal chemistry. The compound may participate in various chemical reactions, including nucleophilic additions and condensation reactions, due to the electrophilic nature of the carbonyl groups. Its potential applications could span across pharmaceuticals, agrochemicals, and materials science, although specific uses would depend on further research into its properties and biological effects. As with many organic compounds, safety precautions should be taken when handling it, as it may pose health risks if ingested or inhaled.

Formula: C₁₆H₉ClO₂

2-[(4-chlorophenyl)methylene]-1H-indene-1,3(2H)-dione

CAS: 15875-54-4

Formula: C₁₆H₉ClO₂

Molecular weight: 268.6945

Ref: IN-DA001QUG

2-((4-Chlorophenyl)methylene)indane-1,3-dione

CAS: 15875-54-4

2-((4-Chlorophenyl)methylene)indane-1,3-dione is an electron acceptor for organic solar cells. It has been shown to outperform other electron acceptors in efficiency and operational stability. This additive can be evaporated to form a uniform layer on the surface of the donor material, which improves light absorption and morphology. 2-((4-Chlorophenyl)methylene)indane-1,3-dione has been shown to be volatile and is therefore suitable for use in solar cells that require a high degree of flexibility, such as polymer solar cells.

Formula: C₁₆H₉ClO₂

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 268.69 g/mol

Ref: 3D-FC169058