4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1-tosyl-1,2,3,6-tetrahydropyridine
97%
- Product Code: 114882
CAS:
1256360-46-9
| Molecular Weight: | 363.28 g./mol | Molecular Formula: | C₁₈H₂₆BNO₄S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD17926518 | |
| Melting Point: | Boiling Point: | 444.2±55.0°C at 760 mmHg | |
| Density: | 1.2±0.1 g/cm3 | Storage Condition: | -20°C, dry sealed |
Product Description:
This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key intermediate for constructing complex molecules. Its boronate ester group facilitates the formation of carbon-carbon bonds, making it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the synthesis of heterocyclic compounds, which are essential in drug discovery and medicinal chemistry. The tosyl group enhances stability and reactivity, enabling precise control in multi-step synthetic processes. Its applications extend to material science, where it contributes to the creation of organic electronic components and functional polymers.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿288.00 |
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| 0.250 | 10-20 days | ฿423.00 |
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| 1.000 | 10-20 days | ฿1,530.00 |
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| 5.000 | 10-20 days | ฿6,219.00 |
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4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1-tosyl-1,2,3,6-tetrahydropyridine
This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key intermediate for constructing complex molecules. Its boronate ester group facilitates the formation of carbon-carbon bonds, making it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the synthesis of heterocyclic compounds, which are essential in drug discovery and medicinal chemistry. The tosyl group enhances stability and reactivity, enabling precise control in multi-step synthetic processes. Its applications extend to material science, where it contributes to the creation of organic electronic components and functional polymers.
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