6711-68-8

Usage

Explanation

The compound's systematic name according to IUPAC nomenclature.

Explanation

An alternative name for the compound, often used in scientific literature.

Explanation

The compound features a unique structure that includes both furan (an oxygen-containing five-membered ring) and pyrrole (a nitrogen-containing five-membered ring) fused together.

Explanation

The compound is typically found in a solid state and exhibits a yellow color.

Explanation

Due to its unique structure, 1H-Furo[3,4-c]pyrrole-1,3(5H)-dione is used as a building block or intermediate in the synthesis of various organic compounds and pharmaceuticals.

Explanation

The compound's intriguing electronic properties make it a candidate for research in the development of organic electronic devices, such as organic light-emitting diodes (OLEDs) or organic solar cells.

Explanation

1H-Furo[3,4-c]pyrrole-1,3(5H)-dione has demonstrated promising antioxidant and anti-inflammatory activities, which could be useful in the development of new drugs for various medical conditions.

Structure

Heterocyclic compound with furan and pyrrole rings

Physical State

Yellow solid

Applications

Synthesis of organic compounds and pharmaceuticals

Electronic Properties

Potential application in organic electronic devices

Biological Activities

Antioxidant and anti-inflammatory

Upstream product

• 935-72-8 pyrrol-3,4-di-carboxylic acid 

Downstream Products

• 133341-91-0 2-benzylpyrrolo<3,4-c>pyrrole-1,3(2H,5H)-dione 
• 133341-90-9 2-methylpyrrolo<3,4-c>pyrrole-1,3(2H,5H)-dione 
• 133341-89-6 4-(benzylcarbamoyl)pyrrole-3-carboxylic acid 

Relevant academic research and scientific papers

Evaluating the influence of heteroatoms on the electronic properties of aryl[3,4-c]pyrroledione based copolymers

A donor-acceptor-type conjugated copolymer (PBDT-PPD) composed of benzodithiophene (BDT) and pyrrolopyrroledione (PPD) was synthesized using the Stille cross-coupling reaction. Using both experimental and theoretical data, the optical, electrochemical, and photovoltaic properties of PBDT-PPD were compared with those of its sulfur analog, PBDT-TPD, which is composed of BDT and thienopyrroledione (TPD). The optical bandgaps of the polymers were determined to be 1.86 and 2.20 eV, respectively. While both materials possessed similar highest occupied molecular orbital (HOMO) levels, the lowest unoccupied molecular orbital (LUMO) level for PBDT-PPD was raised relative to that of PBDT-TPD. Devices incorporating PBDT-PPD had a higher open-circuit voltage and fill factor, yet drastically lower short-circuit current density (Jsc) than PBDT-TPD leading to a lower power conversion efficiency (PCE). The lack of significant intramolecular charge transfer (ICT) combined with the high LUMO of PBDT-PPD resulted in poor spectral overlap with the solar spectrum, lowering Jsc. Additionally, there was poor electron injection into PCBM, which also reduced the PCE.

Organic light-emitting compound and preparation method and application thereof

The invention discloses an organic light-emitting compound as well as a preparation method and application thereof. The organic light-emitting compound has a structural formula shown in the specification, wherein in the structural formula, R is C6-C12 alkyl. According to the preparation method, 2-alkylpyrrolo[3,4-c]pyrrole-1-3(2H, 5H)-diketone is taken as a main body, and chromophoric groups, indole, are respectively introduced into symmetrical positions on two sides of pyrrole, and thereby the organic light-emitting compound is finally obtained. The organic light-emitting compound has a light-emitting characteristic in an organic solvent, wherein the fluorescence intensity is further improved after anions are introduced into a system; the organic light-emitting compound can be applied tothe fields of light-emitting devices, laser dyes, fluorescence sensitivity, anti-counterfeiting technologies, fluorescence imaging, biomedical analysis and the like.

Preparation of Some Pyrrole-3,4-dicarboxylic Acid Derivatives and the Crystal Structure of 2-Methylpyrrolopyrrole-1,3(2H,5H)-dione

A series of pyrrole-3,4-dicarboxylic acid derivatives has been prepared, and the crystal structure of one, 2-methylpyrrolopyrrole-1,3(2H,5H)-dione, has been determined by X-ray diffraction and refined to a residual R 0.049 for 1415 observed reflections.Crystals are monoclinic, space group P21/c, with Z = 8 in a cell of dimensions a 14.775(3), b 7.0692(5), c 15.151(3) Angstroem, β 118.82(8) deg.Strain in the planar fused ring system is evident from the widening of the external interring angles to 143 deg, and from the unusual substituent effects in the 13C n.m.r. spectra.