tert-Butyl (5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)carbamate
97%
- Product Code: 49462
CAS:
910462-31-6
| Molecular Weight: | 320.1917 g./mol | Molecular Formula: | C₁₆H₂₅BN₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD07781162 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction, which is widely employed in the pharmaceutical and materials science industries. Its boronate ester group acts as a key intermediate, enabling the formation of carbon-carbon bonds. This makes it valuable in the development of complex molecules, including drug candidates and advanced materials. Additionally, its pyridine moiety offers versatility in creating heterocyclic compounds, which are often found in bioactive molecules. The tert-butyl carbamate group provides stability and protection during synthetic processes, ensuring efficient and selective reactions. Overall, it is a crucial building block in medicinal chemistry and material design.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $19.71 |
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tert-Butyl (5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)carbamate
This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction, which is widely employed in the pharmaceutical and materials science industries. Its boronate ester group acts as a key intermediate, enabling the formation of carbon-carbon bonds. This makes it valuable in the development of complex molecules, including drug candidates and advanced materials. Additionally, its pyridine moiety offers versatility in creating heterocyclic compounds, which are often found in bioactive molecules. The tert-butyl carbamate group provides stability and protection during synthetic processes, ensuring efficient and selective reactions. Overall, it is a crucial building block in medicinal chemistry and material design.
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