tert-Butyl(2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)ethyl)carbamate
98%
- Product Code: 155764
CAS:
1850305-79-1
| Molecular Weight: | 271.16 g./mol | Molecular Formula: | C₁₃H₂₆BNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD27936408 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature |
Product Description:
Widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key intermediate for introducing boron-containing groups into organic molecules. Its primary application lies in the preparation of pharmaceuticals and agrochemicals, where it enables the formation of carbon-carbon bonds under mild conditions. The tert-butyl carbamate (Boc) protecting group ensures stability of the amine functionality during coupling, allowing selective reactivity at the boron site. After coupling, the Boc group can be easily removed to liberate the amine for further transformations. This makes the compound valuable in multi-step synthesis of complex bioactive molecules, including drug candidates and functional materials.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿1,280.00 |
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| 250mg | 10-20 days | ฿1,490.00 |
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| 1g | 10-20 days | ฿3,800.00 |
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tert-Butyl(2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)ethyl)carbamate
Widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key intermediate for introducing boron-containing groups into organic molecules. Its primary application lies in the preparation of pharmaceuticals and agrochemicals, where it enables the formation of carbon-carbon bonds under mild conditions. The tert-butyl carbamate (Boc) protecting group ensures stability of the amine functionality during coupling, allowing selective reactivity at the boron site. After coupling, the Boc group can be easily removed to liberate the amine for further transformations. This makes the compound valuable in multi-step synthesis of complex bioactive molecules, including drug candidates and functional materials.
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