tert-Butyl 3-methyl-4-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,3,6-tetrahydropyridine-1-carboxylate
97%
- Product Code: 150771
CAS:
1268816-61-0
| Molecular Weight: | 323.24 g./mol | Molecular Formula: | C₁₇H₃₀BNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD22380659 | |
| Melting Point: | Boiling Point: | 358.4±52.0 °C(Predicted) | |
| Density: | 1.04±0.1 g/cm3(Predicted) | Storage Condition: | Room temperature |
Product Description:
Used as an intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. The boronate ester group facilitates carbon-carbon bond formation under mild conditions, making it valuable for constructing substituted tetrahydropyridine scaffolds found in bioactive compounds. Its protected amine function allows for selective reactivity and compatibility with multi-step synthetic sequences.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $463.85 |
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| 0.250 | 10-20 days | $740.88 |
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| 1.000 | 10-20 days | $1,542.58 |
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tert-Butyl 3-methyl-4-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,3,6-tetrahydropyridine-1-carboxylate
Used as an intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. The boronate ester group facilitates carbon-carbon bond formation under mild conditions, making it valuable for constructing substituted tetrahydropyridine scaffolds found in bioactive compounds. Its protected amine function allows for selective reactivity and compatibility with multi-step synthetic sequences.
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