5-(3-Furyl)thiophene-2-boronic acid pinacol ester
95%
- Product Code: 90778
CAS:
2223011-14-9
| Molecular Weight: | 294.17426 g./mol | Molecular Formula: | C₁₄H₁₉BO₄S |
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| Density: | Storage Condition: | -20°C, sealed, dry |
Product Description:
This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a key building block for constructing complex organic molecules, especially in the development of pharmaceuticals and agrochemicals. Its boronic ester group facilitates the formation of carbon-carbon bonds, making it valuable in creating heterocyclic compounds. Additionally, it is employed in material science for synthesizing conjugated polymers, which are essential in organic electronics like OLEDs and solar cells. Its furyl and thiophene moieties contribute to the electronic properties of the resulting materials, enhancing their performance in optoelectronic applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | ฿28,080.00 |
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| 0.100 | 10-20 days | ฿87,120.00 |
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5-(3-Furyl)thiophene-2-boronic acid pinacol ester
This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a key building block for constructing complex organic molecules, especially in the development of pharmaceuticals and agrochemicals. Its boronic ester group facilitates the formation of carbon-carbon bonds, making it valuable in creating heterocyclic compounds. Additionally, it is employed in material science for synthesizing conjugated polymers, which are essential in organic electronics like OLEDs and solar cells. Its furyl and thiophene moieties contribute to the electronic properties of the resulting materials, enhancing their performance in optoelectronic applications.
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