5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-2,2'-bithiophene
≥98%
- Product Code: 71156
CAS:
479719-88-5
| Molecular Weight: | 292.22 g./mol | Molecular Formula: | C₁₄H₁₇BO₂S₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD04039974 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
Widely used in organic electronics, particularly in the synthesis of conjugated polymers and small molecules for organic photovoltaics (OPVs) and organic light-emitting diodes (OLEDs). Its boronate ester group facilitates Suzuki-Miyaura cross-coupling reactions, enabling the creation of complex π-conjugated systems essential for efficient charge transport in these devices. Additionally, it serves as a key intermediate in the development of semiconducting materials for field-effect transistors (FETs), contributing to advancements in flexible and printable electronics. Its thiophene backbone enhances stability and electronic properties, making it a valuable component in high-performance optoelectronic applications.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Green to Blue powder to lump |
| PURITY | 98-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | ฿1,680.00 |
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| 1.000 | 10-20 days | ฿6,980.00 |
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5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-2,2'-bithiophene
Widely used in organic electronics, particularly in the synthesis of conjugated polymers and small molecules for organic photovoltaics (OPVs) and organic light-emitting diodes (OLEDs). Its boronate ester group facilitates Suzuki-Miyaura cross-coupling reactions, enabling the creation of complex π-conjugated systems essential for efficient charge transport in these devices. Additionally, it serves as a key intermediate in the development of semiconducting materials for field-effect transistors (FETs), contributing to advancements in flexible and printable electronics. Its thiophene backbone enhances stability and electronic properties, making it a valuable component in high-performance optoelectronic applications.
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