5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene-2-carboxylic acid
95%
- Product Code: 242341
CAS:
779335-05-6
| Molecular Weight: | 254.11 g./mol | Molecular Formula: | C₁₁H₁₅BO₄S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09952060 | |
| Melting Point: | 176-181°C | Boiling Point: | 403.4°C at 760 mmHg |
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
Used as a key building block in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of conjugated organic materials for applications in organic electronics such as organic light-emitting diodes (OLEDs), organic photovoltaics (OPVs), and conductive polymers. Its boronic ester group facilitates efficient carbon-carbon bond formation with aryl halides, making it valuable in pharmaceutical and agrochemical research for constructing complex thiophene-based structures. The carboxylic acid functionality allows for further derivatization or attachment to surfaces and macromolecules, expanding its utility in material science and bioconjugation.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1g | 10-20 days | ฿6,550.00 |
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| 5g | 10-20 days | ฿26,360.00 |
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5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene-2-carboxylic acid
Used as a key building block in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of conjugated organic materials for applications in organic electronics such as organic light-emitting diodes (OLEDs), organic photovoltaics (OPVs), and conductive polymers. Its boronic ester group facilitates efficient carbon-carbon bond formation with aryl halides, making it valuable in pharmaceutical and agrochemical research for constructing complex thiophene-based structures. The carboxylic acid functionality allows for further derivatization or attachment to surfaces and macromolecules, expanding its utility in material science and bioconjugation.
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