Description
4,7-Dibromo-5,6-bis(hexyloxy)benzo[c][1,2,5]thiadiazole (CAS: 1190978-94-9) is a high-purity organic compound with the molecular formula C18H26Br2N2O2S. This specialized chemical features a benzothiadiazole core functionalized with bromine atoms at the 4 and 7 positions and hexyloxy groups at the 5 and 6 positions, making it an excellent building block for organic electronics and optoelectronic materials. Its unique structure enables applications in polymer solar cells, organic light-emitting diodes (OLEDs), and other advanced material research. This product is rigorously tested for quality and consistency, ensuring optimal performance in research and industrial applications.
Available in various quantities, our 4,7-Dibromo-5,6-bis(hexyloxy)benzo[c][1,2,5]thiadiazole is ideal for researchers and scientists working in materials science, photovoltaics, and synthetic chemistry. Store in a cool, dry place away from light and moisture to maintain stability.
Properties
- CAS Number: 1190978-94-9
- Complexity: 336
- IUPAC Name: 4,7-dibromo-5,6-dihexoxy-2,1,3-benzothiadiazole
- InChI: InChI=1S/C18H26Br2N2O2S/c1-3-5-7-9-11-23-17-13(19)15-16(22-25-21-15)14(20)18(17)24-12-10-8-6-4-2/h3-12H2,1-2H3
- InChI Key: PTSISHLHJISGOZ-UHFFFAOYSA-N
- Exact Mass: 494.00613
- Molecular Formula: C18H26Br2N2O2S
- Molecular Weight: 494.3
- SMILES: CCCCCCOC1=C(C2=NSN=C2C(=C1OCCCCCC)Br)Br
- Topological: 72.5
- Monoisotopic Mass: 492.00817
- Synonyms: 1190978-94-9, 4,7-dibromo-5,6-bis(hexyloxy)benzo[c][1,2,5]thiadiazole, 4,7-Dibromo-5,6-dihexoxy-2,1,3-benzothiadiazole, 2,1,3-Benzothiadiazole, 4,7-dibromo-5,6-bis(hexyloxy)-, 4,7-Dibromo-5,6-bis(hexyloxy)-2,1,3-benzothiadiazole,, 4,7-diBromo-5,6-bis(hexyloxy)benzo[c][1,2,5]thiazole, MFCD28053756, C18H26Br2N2O2S, DTXSID701219592, AKOS027253840, DS-10338, DB-099594, CS-0038562, 4,7-Dibromo-5,6-bis(hexyloxy)-2,1,3-benzothiadiazole
This compound is widely used as a key intermediate in the synthesis of conjugated polymers for organic photovoltaic (OPV) devices due to its electron-accepting properties. It serves as a critical monomer in the development of low-bandgap polymers for high-efficiency solar cells. Additionally, researchers utilize it in the fabrication of OLEDs and other optoelectronic devices to enhance charge transport and light absorption. Its solubility in organic solvents makes it suitable for solution-processed thin-film applications.
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