(3,3'''-Dihexyl-[2,2':5',2'':5'',2'''-quaterthiophene]-5,5'''-diyl)bis(trimethylstannane)
98%
- Product Code: 93968
CAS:
1334669-56-5
| Molecular Weight: | 824.4400000000001 g./mol | Molecular Formula: | C₃₄H₅₀S₄Sn₂ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily used in the field of organic electronics, particularly in the development of organic semiconductors. It serves as a key precursor in the synthesis of conjugated polymers and small molecules, which are essential components in organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). The compound’s structure, featuring quaterthiophene units, enables efficient charge transport, making it valuable for creating high-performance electronic devices. Additionally, its trimethylstannane groups facilitate cross-coupling reactions, such as Stille coupling, which are widely employed in the fabrication of π-conjugated materials for flexible and lightweight electronic applications.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Light yellow to Yellow Solid |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,770.00 |
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(3,3'''-Dihexyl-[2,2':5',2'':5'',2'''-quaterthiophene]-5,5'''-diyl)bis(trimethylstannane)
This chemical is primarily used in the field of organic electronics, particularly in the development of organic semiconductors. It serves as a key precursor in the synthesis of conjugated polymers and small molecules, which are essential components in organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). The compound’s structure, featuring quaterthiophene units, enables efficient charge transport, making it valuable for creating high-performance electronic devices. Additionally, its trimethylstannane groups facilitate cross-coupling reactions, such as Stille coupling, which are widely employed in the fabrication of π-conjugated materials for flexible and lightweight electronic applications.
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