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CAS 566939-58-0

:

1,3-Dibromo-5-octyl-4H-thieno[3,4-c]pyrrole-4,6(5H)-dione

Description:
1,3-Dibromo-5-octyl-4H-thieno[3,4-c]pyrrole-4,6(5H)-dione is a synthetic organic compound characterized by its unique thieno[3,4-c]pyrrole structure, which incorporates a thieno ring fused to a pyrrole moiety. This compound features two bromine substituents at the 1 and 3 positions, enhancing its reactivity and potential applications in organic electronics and materials science. The presence of the octyl group at the 5 position contributes to its solubility and hydrophobic properties, making it suitable for various formulations. The diketone functional groups at positions 4 and 6 are significant for its reactivity, allowing for potential interactions in polymerization or coordination chemistry. This compound is of interest in the field of organic semiconductors, particularly in the development of organic photovoltaic devices and organic light-emitting diodes (OLEDs), due to its electronic properties and ability to form π-stacking interactions. Its stability and performance in these applications can be influenced by the bromine and octyl substituents, which modulate its electronic characteristics and solubility.
Formula:C14H17Br2NO2S
InChI:InChI=1S/C14H17Br2NO2S/c1-2-3-4-5-6-7-8-17-13(18)9-10(14(17)19)12(16)20-11(9)15/h2-8H2,1H3
InChI key:InChIKey=GSGMEQUXTCYOAU-UHFFFAOYSA-N
SMILES:O=C1C=2C(C(=O)N1CCCCCCCC)=C(Br)SC2Br
Synonyms:
  • 1,3-Dibromo-5-octylthieno[3,4-c]pyrrole-4,6-dione
  • 4H-Thieno[3,4-c]pyrrole-4,6(5H)-dione, 1,3-dibromo-5-octyl-
  • K0260
  • Thieno[3,4-c]pyrole-4,6-dione
  • 1,3-Dibromo-5-octyl-4H-thieno[3,4-c]pyrrole-4,6(5H)-dione
  • 1,3-Dibromo-5-octyl-4H-thieno[3,4-c]pyrrole-4,6-(5H)-dione
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