tert-butyl (4-((4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)methylene)cyclohexyl)carbamate
98%
- Product Code: 242152
CAS:
2694028-09-4
| Molecular Weight: | 337.27 g./mol | Molecular Formula: | C₁₈H₃₂BNO₄ |
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| EC Number: | MDL Number: | ||
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| Density: | Storage Condition: | 2-8℃ |
Product Description:
Used in organic synthesis as a protected amine-containing boronic ester derivative, enabling Suzuki-Miyaura cross-coupling reactions in the construction of complex organic molecules, particularly in pharmaceutical and agrochemical research. The tert-butyl carbamate group acts as a protecting group for the amine, allowing selective reactivity at the boronic ester site. This compound is valuable for synthesizing functionalized amines and cyclic frameworks found in bioactive compounds. Its structure supports the development of drug candidates by facilitating carbon-carbon bond formation under mild palladium-catalyzed conditions.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.010 | 10-20 days | ฿2,510.00 |
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| 0.100 | 10-20 days | ฿17,460.00 |
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| 0.500 | 10-20 days | ฿52,380.00 |
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| 1.000 | 10-20 days | ฿70,460.00 |
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tert-butyl (4-((4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)methylene)cyclohexyl)carbamate
Used in organic synthesis as a protected amine-containing boronic ester derivative, enabling Suzuki-Miyaura cross-coupling reactions in the construction of complex organic molecules, particularly in pharmaceutical and agrochemical research. The tert-butyl carbamate group acts as a protecting group for the amine, allowing selective reactivity at the boronic ester site. This compound is valuable for synthesizing functionalized amines and cyclic frameworks found in bioactive compounds. Its structure supports the development of drug candidates by facilitating carbon-carbon bond formation under mild palladium-catalyzed conditions.
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