tert-butyl 3-((4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)methylene)piperidine-1-carboxylate
99%
- Product Code: 242150
CAS:
2376764-47-3
| Molecular Weight: | 323.24 g./mol | Molecular Formula: | C₁₇H₃₀BNO₄ |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8℃ |
Product Description:
Widely used in cross-coupling reactions, particularly in Suzuki-Miyaura coupling, this compound serves as a key intermediate in the synthesis of complex organic molecules. Its boron-containing group enables efficient carbon-carbon bond formation, making it valuable in pharmaceutical and agrochemical research. The tert-butyl carbamate-protected piperidine structure allows for selective transformations in multi-step syntheses, especially in drug discovery where nitrogen-containing heterocycles are common. After coupling, the protecting group can be easily removed under mild acidic conditions, enabling further functionalization. Its stability and reactivity profile make it a preferred building block in medicinal chemistry and process development.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿6,860.00 |
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| 0.500 | 10-20 days | ฿18,000.00 |
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| 1.000 | 10-20 days | ฿29,650.00 |
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| 5.000 | 10-20 days | ฿88,950.00 |
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tert-butyl 3-((4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)methylene)piperidine-1-carboxylate
Widely used in cross-coupling reactions, particularly in Suzuki-Miyaura coupling, this compound serves as a key intermediate in the synthesis of complex organic molecules. Its boron-containing group enables efficient carbon-carbon bond formation, making it valuable in pharmaceutical and agrochemical research. The tert-butyl carbamate-protected piperidine structure allows for selective transformations in multi-step syntheses, especially in drug discovery where nitrogen-containing heterocycles are common. After coupling, the protecting group can be easily removed under mild acidic conditions, enabling further functionalization. Its stability and reactivity profile make it a preferred building block in medicinal chemistry and process development.
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