5-(4-Fluoro-2-methylphenyl)thiophene-2-boronic acid pinacol ester
95%
- Product Code: 90794
CAS:
1402227-73-9
| Molecular Weight: | 336.2291832 g./mol | Molecular Formula: | C₁₇H₂₂BFO₃S |
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| Density: | Storage Condition: | -20°C, sealed, dry |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex organic molecules, especially in the pharmaceutical and agrochemical industries. The boronic ester group facilitates the formation of carbon-carbon bonds, enabling the synthesis of biaryl structures, which are common in active pharmaceutical ingredients. Its specific structure, including the fluorine and methyl substituents, allows for fine-tuning of electronic and steric properties, making it valuable in designing molecules with targeted biological activities. Additionally, it is employed in material science for developing organic electronic materials, such as organic light-emitting diodes (OLEDs) and semiconductors, due to its conjugated thiophene moiety.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.005 | 10-20 days | ฿8,982.00 |
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| 0.025 | 10-20 days | ฿19,800.00 |
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5-(4-Fluoro-2-methylphenyl)thiophene-2-boronic acid pinacol ester
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex organic molecules, especially in the pharmaceutical and agrochemical industries. The boronic ester group facilitates the formation of carbon-carbon bonds, enabling the synthesis of biaryl structures, which are common in active pharmaceutical ingredients. Its specific structure, including the fluorine and methyl substituents, allows for fine-tuning of electronic and steric properties, making it valuable in designing molecules with targeted biological activities. Additionally, it is employed in material science for developing organic electronic materials, such as organic light-emitting diodes (OLEDs) and semiconductors, due to its conjugated thiophene moiety.
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