1057401-13-4 | 3,6-Bis(5-bromothiophen-2-yl)-2,5-dioctylpyrrolo[3,4-c]pyrrole-1,4(2H,5H)-dione

Packsize	Purity	Availability	Price	Discounted Price
100mg	95%	1 week	$62.00	$44.00
250mg	95%	1 week	$106.00	$74.00
1g	95%	1 week	$284.00	$199.00

Description

• Catalog Number: AE17153
• Chemical Name: 3,6-Bis(5-bromothiophen-2-yl)-2,5-dioctylpyrrolo[3,4-c]pyrrole-1,4(2H,5H)-dione
• CAS Number: 1057401-13-4
• Molecular Formula: C30H38Br2N2O2S2
• Molecular Weight: 682.5729
• MDL Number: MFCD16619389
• SMILES: CCCCCCCCn1c(=O)c2c(c1c1ccc(s1)Br)c(=O)n(c2c1ccc(s1)Br)CCCCCCCC

Upstream Synthesis Route

The compound 3,6-Bis(5-bromothiophen-2-yl)-2,5-dioctylpyrrolo[3,4-c]pyrrole-1,4(2H,5H)-dione has significant utility in chemical synthesis as a versatile building block. Its unique structure, featuring multiple thiophene rings and a pyrrolopyrrole core, provides it with diverse reactivity and properties that make it highly valuable in creating novel organic compounds.One important application of this compound in chemical synthesis is its use as a key intermediate in the production of organic semiconductors. By incorporating 3,6-Bis(5-bromothiophen-2-yl)-2,5-dioctylpyrrolo[3,4-c]pyrrole-1,4(2H,5H)-dione into the molecular structure of semiconductor materials, researchers can tailor the electronic properties of the final product. This enables the design and fabrication of advanced electronic devices such as organic field-effect transistors and solar cells.Furthermore, the presence of bromine atoms on the thiophene rings offers the potential for further functionalization through cross-coupling reactions, allowing chemists to introduce additional substituents or linkages to fine-tune the properties of the synthesized compounds. This flexibility in derivatization expands the scope of applications for 3,6-Bis(5-bromothiophen-2-yl)-2,5-dioctylpyrrolo[3,4-c]pyrrole-1,4(2H,5H)-dione in organic chemistry and materials science.