4-(2-Ethylhexyl)-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene
≥97%
- Product Code: 183117
CAS:
1224430-50-5
| Molecular Weight: | 322.31 g./mol | Molecular Formula: | C₁₈H₃₁BO₂S |
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| Density: | Storage Condition: | 2-8°C |
Product Description:
Used primarily in organic synthesis, especially in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key building block for constructing conjugated thiophene-based materials. Its boronate ester group enables efficient carbon-carbon bond formation with aryl or heteroaryl halides, making it valuable in the development of organic semiconductors, conductive polymers, and π-conjugated systems. It is commonly employed in the synthesis of organic electronic materials, including those used in organic light-emitting diodes (OLEDs), organic photovoltaics (OPVs), and field-effect transistors (OFETs). The 2-ethylhexyl substituent enhances solubility in organic solvents, which improves processability in thin-film device fabrication.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 200mg | 10-20 days | ฿2,160.00 |
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| 1g | 10-20 days | ฿8,070.00 |
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4-(2-Ethylhexyl)-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene
Used primarily in organic synthesis, especially in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key building block for constructing conjugated thiophene-based materials. Its boronate ester group enables efficient carbon-carbon bond formation with aryl or heteroaryl halides, making it valuable in the development of organic semiconductors, conductive polymers, and π-conjugated systems. It is commonly employed in the synthesis of organic electronic materials, including those used in organic light-emitting diodes (OLEDs), organic photovoltaics (OPVs), and field-effect transistors (OFETs). The 2-ethylhexyl substituent enhances solubility in organic solvents, which improves processability in thin-film device fabrication.
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