| Identification | Back Directory | [Name]
3,6-Di(2-thienyl)-2,5-dihydropyrrolo[3,4-c]pyrrole-1,4-dione | [CAS]
850583-75-4 | [Synonyms]
S8170
3,6-Di(thiophen-2-yl)pyrrolo[3,4-c]pyrrole-1,5-dione
3,6-Di(2-thienyl)pyrrolo[3,4-c]pyrrole-1,4(2H,5H)-dione
3,6-Di(2-thienyl)-2,5-dihydropyrrolo[3,4-c]pyrrole-1,4-dion
2,5-Dihydro-3,6-di-2-thienyl-pyrrolo[3,4-c]pyrrole-1,4-dione
IN1323, 3,6-Di(thiophen-2-yl)pyrrolo[3,4-c]pyrrole-1,4-dione
3,6-Di(2-thienyl)-2,5-dihydropyrrolo[3,4-c]pyrrole-1,4-dione
Pyrrolo[3,4-c]pyrrole-1,4-dione, 2,5-dihydro-3,6-di-2-thienyl-
3,6-Dithiophen-2-yl-2,5-dihydropyrrolo[3,4-c]pyrrole-1,4-dione
3,6-Di(2-thienyl)-2,5-dihydropyrrolo[3,4-c]pyrrole-1,4-dione>
2,5-Dihydro-3,6-di-2-thienyl-pyrrolo[3,4-c]pyrrole-1,4-dione 97%
3,6-Di(thiophen-2-yl)pyrrolo[3,4-c]pyrrole-2,5-dihydro-1,4-dione
2,5-Dihydro-3,6-di-2-thienyl-pyrrolo[3,4-c]pyrrole-1,4-dione (DPP)
3,6-Di(2-thienyl)-2,5-dihydropyrrolo[3,4-c]pyrrole-1,4-dione
850583-75-4 3,6-Di(2-thienyl)-2,5-dihydropyrrolo[3,4-c]pyrrole-1,4-dione | [Molecular Formula]
C14H8N2O2S2 | [MDL Number]
MFCD20257907 | [MOL File]
850583-75-4.mol | [Molecular Weight]
300.356 |
| Chemical Properties | Back Directory | [Boiling point ]
691.9±55.0 °C(Predicted) | [density ]
1.60±0.1 g/cm3(Predicted) | [storage temp. ]
Keep in dark place,Sealed in dry,Room Temperature | [form ]
powder to crystal | [pka]
8.13±0.60(Predicted) | [color ]
Dark green to Dark red to Black | [InChI]
InChI=1S/C14H8N2O2S2/c17-13-9-10(12(16-13)8-4-2-6-20-8)14(18)15-11(9)7-3-1-5-19-7/h1-6H,(H,15,18)(H,16,17) | [InChIKey]
YIUHGBNJJRTMIE-UHFFFAOYSA-N | [SMILES]
N1C(C2SC=CC=2)=C2C(=O)NC(C3SC=CC=3)=C2C1=O |
| Hazard Information | Back Directory | [Uses]
suzuki reaction | [General Description]
2,5-Dihydro-3,6-di-2-thienyl-pyrrolo[3,4-c]pyrrole-1,4-dione is a diketopyrrolopyrrole (DPP) based copolymer and are used widely in thin-film transistors and solar cell devices. This aromatic polymer has electron withdrawing groups and hence is very useful for the synthesis of narrow band gap donor-acceptor polymers which are used as active semiconductors for organic electronics. They give rise to high power conversion efficiency (PCE) in Organic Photovoltaic (OPV) Cells. |
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