5-N-Propylthiophene-2-Boronic Acid Pinacol Este
95%
- Product Code: 90871
CAS:
1473358-18-7
| Molecular Weight: | 252.19 g./mol | Molecular Formula: | C₁₃H₂₁BO₂S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18436112 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, which are essential for creating carbon-carbon bonds in the production of pharmaceuticals, agrochemicals, and organic materials. Its boronic ester group makes it a stable and effective reagent for introducing the thiophene moiety into complex molecules, enabling the development of compounds with specific electronic or structural properties. Additionally, it finds application in the synthesis of conjugated polymers and small molecules for organic electronics, such as organic light-emitting diodes (OLEDs) and organic photovoltaics, due to its ability to facilitate the formation of thiophene-based architectures.
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-N-Propylthiophene-2-Boronic Acid Pinacol Este
This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, which are essential for creating carbon-carbon bonds in the production of pharmaceuticals, agrochemicals, and organic materials. Its boronic ester group makes it a stable and effective reagent for introducing the thiophene moiety into complex molecules, enabling the development of compounds with specific electronic or structural properties. Additionally, it finds application in the synthesis of conjugated polymers and small molecules for organic electronics, such as organic light-emitting diodes (OLEDs) and organic photovoltaics, due to its ability to facilitate the formation of thiophene-based architectures.
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