tert-Butyl 2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-5,6-dihydropyridine-1(2H)-carboxylate
95%
- Product Code: 115508
CAS:
1005397-65-8
| Molecular Weight: | 337.26 g./mol | Molecular Formula: | C₁₈H₃₂BNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD14582863 | |
| Melting Point: | Boiling Point: | 368.8±52.0 °C(Predicted) | |
| Density: | 1.03±0.1 g/cm3(Predicted) | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This chemical is primarily utilized in organic synthesis as a versatile building block, particularly in cross-coupling reactions. Its boronate ester group makes it valuable in Suzuki-Miyaura coupling, a widely used method for forming carbon-carbon bonds. This reaction is essential in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. The compound’s structure, featuring a protected amine group, allows for selective functionalization, enabling the construction of diverse heterocyclic frameworks. Its stability and reactivity make it a preferred intermediate in medicinal chemistry for developing drug candidates. Additionally, it is employed in the preparation of boron-containing compounds, which are increasingly important in materials science and catalysis.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.050 | 10-20 days | $256.26 |
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| 0.100 | 10-20 days | $409.90 |
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| 0.250 | 10-20 days | $696.67 |
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tert-Butyl 2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-5,6-dihydropyridine-1(2H)-carboxylate
This chemical is primarily utilized in organic synthesis as a versatile building block, particularly in cross-coupling reactions. Its boronate ester group makes it valuable in Suzuki-Miyaura coupling, a widely used method for forming carbon-carbon bonds. This reaction is essential in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. The compound’s structure, featuring a protected amine group, allows for selective functionalization, enabling the construction of diverse heterocyclic frameworks. Its stability and reactivity make it a preferred intermediate in medicinal chemistry for developing drug candidates. Additionally, it is employed in the preparation of boron-containing compounds, which are increasingly important in materials science and catalysis.
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