507484-54-0

Usage

Uses

Used in Fluorescent Dyes and Pigments:
2-(6-fluoro-3-oxo-2,3-dihydro-1H-inden-1-ylidene)malononitrile is used as a key component in the development of fluorescent dyes and pigments, leveraging its unique optical properties to enhance the performance of these materials.
Used in Organic Synthesis:
In the field of organic synthesis, 2-(6-fluoro-3-oxo-2,3-dihydro-1H-inden-1-ylidene)malononitrile serves as a valuable intermediate, contributing to the creation of complex organic molecules and compounds.
Used in Materials Science:
2-(6-fluoro-3-oxo-2,3-dihydro-1H-inden-1-ylidene)malononitrile is utilized in materials science for its potential to contribute to the development of advanced materials with specific properties, such as those needed in photonic applications.
Used in Pharmaceutical and Agrochemical Industries:
2-(6-fluoro-3-oxo-2,3-dihydro-1H-inden-1-ylidene)malononitrile is employed as a building block in the synthesis of various pharmaceuticals and agrochemicals, where its unique structure and properties can be harnessed to create novel and effective products.
Used in Photonic Materials:
2-(6-fluoro-3-oxo-2,3-dihydro-1H-inden-1-ylidene)malononitrile is used as a component in photonic materials due to its interesting optical and electronic properties, which can be exploited to develop materials with specific photonic characteristics for various applications.

Upstream product

• 54746-57-5 5-fluoroindene-1,3-dione 
• 109-77-3 malononitrile 

Relevant academic research and scientific papers

Polyquinane-based conjugated macromolecule and preparation method and application thereof

The invention relates to the field of solar cells and optical detectors, in particular to polyquinane-based conjugated macromolecules and a preparation methods and application thereof. The conjugatedmacromolecule is a compound as shown in the formula (1).

Two-dimensional condensed ring conjugate large molecule, and preparation method and application thereof

The invention relates to the field of solar cells and optical detectors, in particular to a two-dimensional condensed ring conjugate large molecule, and a preparation method and application thereof. The two-dimensional condensed ring conjugate large molec

Compound and preparation method thereof and organic photovoltaic device comprising compound

The application provides a compound as shown in a formula I, a preparation method of the compound and an organic photovoltaic device comprising the compound. The formula is shown in the description. In the formula I, R1, R2 and R3 are separately selected from H, C1-C30 alkyl, C3-C30 cycloalkyl, C1-C30 alkoxy, C1-C30 alkyl sulphanyl, C1-C30 halogenated alkyl, C3-C30 halogenated cycloalkyl and C1-C30 halogenated alkoxy; groups of C1-C30 alkyls, C3-C30 cycloalkyls, C1-C30 alkoxys, C1-C30 alkyl sulphanyls, C1-C30 halogenated alkyls, C3-C30 halogenated cycloalkyls and C1-C30 halogenated alkoxys areoptionally substituted by one or more of groups of hydroxyl, cyan, nitryl and halogen; n and m are independently selected from an integer of 0, 1, 2 or 3; A1 and A2 are independently selected from the following groups as shown in the description; the formula is shown in the description. R4, R5, R6 and R7 are independently selected from hydrogen, halogen, C1-C30 alkyl, C3-C30 cycloalkyl, C1-C30 alkoxy or C1-C30 halogenated alkyl; and when n and m are equal to 0 and A1 and A2 are A-A, one or more of R4, R5, R6 and R7 is not hydrogen. The compound as shown in the formula I can be used for an organic photovoltaic material.

Many and fused ring conjugated macromolecule and its preparation method and application (by machine translation)

The present invention relates to organic and perovskite solar cell and optical detectors, in particular, relates to a multi-and fused ring conjugated macromolecule and its preparation method and application. The plurality of and fused ring conjugated macr

Fused nonacyclic electron acceptors for efficient polymer solar cells

We design and synthesize four fused-ring electron acceptors based on 6,6,12,12-tetrakis(4-hexylphenyl)-indacenobis(dithieno[3,2-b;2',3'-d]thiophene) as the electron-rich unit and 1,1-dicyanomethylene-3-indanones with 0-2 fluorine substituents as the elect