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
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
APPEARANCE Red to Purple
PURITY 97.5-100
Infrared spectrum Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
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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