tert-Butyl N-(3-bromo-6-chloropyrazin-2-yl)-N-[(tert-butoxy)carbonyl]carbamate
95%
- Product Code: 53349
CAS:
1801693-41-3
| Molecular Weight: | 408.7 g./mol | Molecular Formula: | C₁₄H₁₉BrClN₃O₄ |
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| Density: | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
This chemical is primarily utilized in the synthesis of complex organic compounds, particularly in pharmaceutical research and development. It serves as a key intermediate in the production of active pharmaceutical ingredients (APIs) and is often employed in the construction of pyrazine-based structures, which are significant in medicinal chemistry. Its functional groups, including the bromo and chloro substituents, make it a versatile building block for cross-coupling reactions, enabling the creation of diverse molecular frameworks. Additionally, the tert-butyl and tert-butoxycarbonyl (Boc) protecting groups enhance its stability during synthetic processes, allowing for selective deprotection and further functionalization. This compound is particularly valuable in the development of drugs targeting various diseases, including cancer and infectious diseases, due to its ability to introduce specific pharmacophores into drug candidates.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $1,649.33 |
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tert-Butyl N-(3-bromo-6-chloropyrazin-2-yl)-N-[(tert-butoxy)carbonyl]carbamate
This chemical is primarily utilized in the synthesis of complex organic compounds, particularly in pharmaceutical research and development. It serves as a key intermediate in the production of active pharmaceutical ingredients (APIs) and is often employed in the construction of pyrazine-based structures, which are significant in medicinal chemistry. Its functional groups, including the bromo and chloro substituents, make it a versatile building block for cross-coupling reactions, enabling the creation of diverse molecular frameworks. Additionally, the tert-butyl and tert-butoxycarbonyl (Boc) protecting groups enhance its stability during synthetic processes, allowing for selective deprotection and further functionalization. This compound is particularly valuable in the development of drugs targeting various diseases, including cancer and infectious diseases, due to its ability to introduce specific pharmacophores into drug candidates.
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