AA56335
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
100mg | 97% | in stock | $64.00 | $45.00 | - + | |
250mg | 97% | in stock | $89.00 | $62.00 | - + | |
1g | 97% | in stock | $195.00 | $137.00 | - + | |
5g | 97% | in stock | $829.00 | $581.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AA56335 |
Chemical Name: | 2,6-Dibromo-4,8-bis((2-ethylhexyl)oxy)benzo[1,2-b:4,5-b']dithiophene |
CAS Number: | 1226782-13-3 |
Molecular Formula: | C26H36Br2O2S2 |
Molecular Weight: | 604.5008 |
MDL Number: | MFCD17018552 |
SMILES: | CCCCC(COc1c2sc(cc2c(c2c1cc(s2)Br)OCC(CCCC)CC)Br)CC |
2,6-Dibromo-4,8-bis((2-ethylhexyl)oxy)benzo[1,2-b:4,5-b']dithiophene is a versatile compound that finds widespread application in chemical synthesis processes. This molecule is particularly valued in the field of organic electronics and materials science due to its unique structural characteristics. In chemical synthesis, 2,6-Dibromo-4,8-bis((2-ethylhexyl)oxy)benzo[1,2-b:4,5-b']dithiophene serves as a crucial building block for the construction of advanced functional materials. By incorporating this compound into the molecular framework of various organic compounds, researchers are able to tailor the properties of the resulting materials to meet specific requirements. One significant application of this compound is in the synthesis of conjugated polymers and oligomers used in the fabrication of organic photovoltaic devices. The presence of the dithiophene and bromine groups in the molecule allows for efficient electron transport and good compatibility with other materials in the device architecture. This enables the development of high-performance organic solar cells with improved efficiency and stability.Furthermore, the ethylhexyl side chains in 2,6-Dibromo-4,8-bis((2-ethylhexyl)oxy)benzo[1,2-b:4,5-b']dithiophene contribute to the solubility and processability of the compound, making it easier to incorporate into solution-based processing techniques such as spin-coating or inkjet printing. This feature is particularly advantageous in large-scale manufacturing processes, where the compound can be applied to flexible substrates to produce lightweight and flexible electronic devices.Overall, the strategic use of 2,6-Dibromo-4,8-bis((2-ethylhexyl)oxy)benzo[1,2-b:4,5-b']dithiophene in chemical synthesis holds great promise for the development of innovative materials with applications ranging from flexible electronics to optoelectronic devices.