methyl4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene-2-carboxylate
≥95%
- Product Code: 46250
CAS:
709648-80-6
| Molecular Weight: | 268.14 g./mol | Molecular Formula: | C₁₂H₁₇BO₄S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD13689007 | |
| Melting Point: | Boiling Point: | 374.6°C at 760 mmHg | |
| Density: | 1.162g/cm3 | Storage Condition: | -20°C, protected from light and stored in an inert gas |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex thiophene-based compounds, which are valuable in the development of pharmaceuticals, agrochemicals, and organic electronic materials. Its boronate ester functional group enables efficient coupling with aryl or vinyl halides, facilitating the creation of carbon-carbon bonds. Additionally, it finds applications in the synthesis of conjugated polymers and small molecules for use in organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs), contributing to advancements in material science and energy technologies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | £113.99 |
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| 0.250 | 10-20 days | £199.28 |
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| 1.000 | 10-20 days | £348.89 |
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methyl4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene-2-carboxylate
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex thiophene-based compounds, which are valuable in the development of pharmaceuticals, agrochemicals, and organic electronic materials. Its boronate ester functional group enables efficient coupling with aryl or vinyl halides, facilitating the creation of carbon-carbon bonds. Additionally, it finds applications in the synthesis of conjugated polymers and small molecules for use in organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs), contributing to advancements in material science and energy technologies.
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