2,7-Bis(trimethylstannyl)naphtho[1,2-b:5,6-b']dithiophene
99%
- Product Code: 123957
CAS:
1218771-02-8
| Molecular Weight: | 565.95 g./mol | Molecular Formula: | C₂₀H₂₄S₂Sn₂ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 538.6±60.0 °C(Predicted) | |
| Density: | Storage Condition: | Room temperature, dark, sealed, dry |
Product Description:
This compound is primarily utilized in the field of organic electronics, particularly in the synthesis of conjugated polymers and small molecules for use in organic photovoltaics (OPVs) and organic field-effect transistors (OFETs). Its structure, featuring a naphthodithiophene core with trimethylstannyl groups, makes it a valuable building block for cross-coupling reactions, such as Stille coupling, which is essential for creating high-performance semiconducting materials. The compound's ability to facilitate efficient charge transport and light absorption in organic semiconductors contributes to the development of flexible, lightweight, and cost-effective electronic devices, including solar cells and displays.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | Solid |
| Purity (%) | 98.5-100 |
| Infrared Spectrum | Conforms To Structure |
| NMR | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿11,280.00 |
+
-
|
| 0.250 | 10-20 days | ฿19,600.00 |
+
-
|
2,7-Bis(trimethylstannyl)naphtho[1,2-b:5,6-b']dithiophene
This compound is primarily utilized in the field of organic electronics, particularly in the synthesis of conjugated polymers and small molecules for use in organic photovoltaics (OPVs) and organic field-effect transistors (OFETs). Its structure, featuring a naphthodithiophene core with trimethylstannyl groups, makes it a valuable building block for cross-coupling reactions, such as Stille coupling, which is essential for creating high-performance semiconducting materials. The compound's ability to facilitate efficient charge transport and light absorption in organic semiconductors contributes to the development of flexible, lightweight, and cost-effective electronic devices, including solar cells and displays.
| Mechanism | - |
| Appearance | - |
| Longevity | - |
| Strength | - |
| Storage | - |
| Shelf Life | - |
| Allergen(s) | - |
| Dosage (Range) | - |
| Recommended Dosage | - |
| Dosage (Per Day) | - |
| Recommended Dosage (Per Day) | - |
| Mix Method | - |
| Heat Resistance | - |
| Stable in pH range | - |
| Solubility | - |
| Product Types | - |
| INCI | - |
Cart
No products
Subtotal:
฿0.00
฿0.00
Total :