4,4'-Dibutoxy-2,2'-bis(trimethylstannyl)-5,5'-bithiazol
98%
- Product Code: 77189
Alias:
3,6-bis(5-bromothiophen-2-yl)-2,5-bis(2-decyltetradecyl)pyrrolo[3,4-c]pyrrole-1,4(2H,5H)- diketone
CAS:
1224430-28-7
Molecular Weight: | 1131.42 g./mol | Molecular Formula: | C₆₂H₁₀₂Br₂N₂O₂S₂ |
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EC Number: | MDL Number: | ||
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily utilized in the field of organic electronics, particularly in the synthesis of conductive polymers and semiconducting materials. Its unique structure, featuring a bithiazole core with stannyl and butoxy groups, makes it a valuable precursor for creating polymers with tailored electronic properties. These polymers are often employed in the fabrication of organic light-emitting diodes (OLEDs), organic photovoltaic cells (OPVs), and other optoelectronic devices. Additionally, the compound's ability to facilitate cross-coupling reactions, such as Stille coupling, allows for the efficient formation of complex conjugated systems, which are essential for high-performance electronic materials. Its application extends to research and development in material science, where it aids in the exploration of novel organic semiconductors with improved efficiency and stability.
Product Specification:
Test | Specification |
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APPEARANCE | Red to Purple |
PURITY | 97.5-100 |
Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.050 | 10-20 days | ฿3,300.00 |
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0.250 | 10-20 days | ฿11,720.00 |
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1.000 | 10-20 days | ฿30,310.00 |
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4,4'-Dibutoxy-2,2'-bis(trimethylstannyl)-5,5'-bithiazol
This chemical is primarily utilized in the field of organic electronics, particularly in the synthesis of conductive polymers and semiconducting materials. Its unique structure, featuring a bithiazole core with stannyl and butoxy groups, makes it a valuable precursor for creating polymers with tailored electronic properties. These polymers are often employed in the fabrication of organic light-emitting diodes (OLEDs), organic photovoltaic cells (OPVs), and other optoelectronic devices. Additionally, the compound's ability to facilitate cross-coupling reactions, such as Stille coupling, allows for the efficient formation of complex conjugated systems, which are essential for high-performance electronic materials. Its application extends to research and development in material science, where it aids in the exploration of novel organic semiconductors with improved efficiency and stability.
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