2-(n-Propyl)thiophene-4-boronic acid pinacol ester
95%
- Product Code: 89667
CAS:
1595111-51-5
| Molecular Weight: | 270.19592 g./mol | Molecular Formula: | C₁₃H₂₃BO₃S |
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| Density: | Storage Condition: | -20°C, sealed, dry |
Product Description:
2-(n-Propyl)thiophene-4-boronic acid pinacol ester is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This compound serves as a key intermediate in the preparation of complex organic molecules, especially in the pharmaceutical and agrochemical industries. Its boronic ester group facilitates the formation of carbon-carbon bonds, making it valuable for constructing biaryl compounds and heterocycles. Additionally, it is employed in the development of organic electronic materials, such as polymers and small molecules for use in OLEDs and organic photovoltaics, due to its thiophene backbone, which enhances electronic properties. Its stability and reactivity under mild conditions make it a preferred choice in various catalytic processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | $2,103.99 |
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| 0.100 | 10-20 days | $6,311.96 |
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2-(n-Propyl)thiophene-4-boronic acid pinacol ester
2-(n-Propyl)thiophene-4-boronic acid pinacol ester is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This compound serves as a key intermediate in the preparation of complex organic molecules, especially in the pharmaceutical and agrochemical industries. Its boronic ester group facilitates the formation of carbon-carbon bonds, making it valuable for constructing biaryl compounds and heterocycles. Additionally, it is employed in the development of organic electronic materials, such as polymers and small molecules for use in OLEDs and organic photovoltaics, due to its thiophene backbone, which enhances electronic properties. Its stability and reactivity under mild conditions make it a preferred choice in various catalytic processes.
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