4,4,5,5-Tetramethyl-2-(5-octylthiophen-2-yl)-1,3,2-dioxaborolane
98%
- Product Code: 242940
CAS:
925424-90-4
| Molecular Weight: | 322.31 g./mol | Molecular Formula: | C₁₈H₃₁BO₂S |
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| EC Number: | MDL Number: | MFCD28360688 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C, light-proof, inert gas |
Product Description:
Used in organic synthesis as a boronic ester coupling partner in Suzuki-Miyaura cross-coupling reactions. It enables the formation of carbon-carbon bonds, particularly in the construction of conjugated thiophene-based polymers and oligomers used in organic electronics. The octyl chain enhances solubility in organic solvents, making it suitable for solution-processable semiconducting materials. Commonly applied in the development of organic photovoltaics (OPVs), field-effect transistors (OFETs), and light-emitting diodes (OLEDs). The borolane ring is stable and selective under coupling conditions, allowing for efficient and selective reactions with aryl or heteroaryl halides in the presence of palladium catalysts.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 250mg | 10-20 days | ฿1,930.00 |
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4,4,5,5-Tetramethyl-2-(5-octylthiophen-2-yl)-1,3,2-dioxaborolane
Used in organic synthesis as a boronic ester coupling partner in Suzuki-Miyaura cross-coupling reactions. It enables the formation of carbon-carbon bonds, particularly in the construction of conjugated thiophene-based polymers and oligomers used in organic electronics. The octyl chain enhances solubility in organic solvents, making it suitable for solution-processable semiconducting materials. Commonly applied in the development of organic photovoltaics (OPVs), field-effect transistors (OFETs), and light-emitting diodes (OLEDs). The borolane ring is stable and selective under coupling conditions, allowing for efficient and selective reactions with aryl or heteroaryl halides in the presence of palladium catalysts.
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