[4,8-Bis[5-(2-octyldodecyl)thiophen-2-yl]-2-trimethylstannylthieno[2,3-f][1]benzothiol-6-yl]-trimethylstannane

98%

  • Product Code: 93986
  CAS:    1709838-53-8
Molecular Weight: 1241.230 g./mol Molecular Formula: C₆₄H₁₀₆S₄Sn₂
EC Number: MDL Number:
Melting Point: Boiling Point:
Density: Storage Condition: 2-8°C, sealed, dry
Product Description: This chemical is primarily utilized in the field of organic electronics, particularly in the development of advanced materials for photovoltaic devices. It serves as a key component in the synthesis of conjugated polymers, which are essential for creating efficient organic solar cells. The compound’s structure, featuring thiophene and benzothiophene units, allows for enhanced light absorption and charge transport properties, making it suitable for use in light-harvesting applications. Additionally, its trimethylstannyl groups facilitate cross-coupling reactions, enabling the formation of high-performance semiconducting polymers. This contributes to the production of flexible, lightweight, and cost-effective solar panels, as well as other optoelectronic devices like organic light-emitting diodes (OLEDs) and field-effect transistors (FETs). Its application in these technologies supports the advancement of renewable energy solutions and next-generation electronic displays.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿20,745.00
+
-
[4,8-Bis[5-(2-octyldodecyl)thiophen-2-yl]-2-trimethylstannylthieno[2,3-f][1]benzothiol-6-yl]-trimethylstannane
This chemical is primarily utilized in the field of organic electronics, particularly in the development of advanced materials for photovoltaic devices. It serves as a key component in the synthesis of conjugated polymers, which are essential for creating efficient organic solar cells. The compound’s structure, featuring thiophene and benzothiophene units, allows for enhanced light absorption and charge transport properties, making it suitable for use in light-harvesting applications. Additionally, its trimethylstannyl groups facilitate cross-coupling reactions, enabling the formation of high-performance semiconducting polymers. This contributes to the production of flexible, lightweight, and cost-effective solar panels, as well as other optoelectronic devices like organic light-emitting diodes (OLEDs) and field-effect transistors (FETs). Its application in these technologies supports the advancement of renewable energy solutions and next-generation electronic displays.
Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Cart

No products

Subtotal: ฿0.00
฿0.00 Total :