N,N-bis-(tert-butoxycarbonyl)-2,5-bis-methoxycarbonyl-1,4-dihydropyrazine
- Product Code: 54512
CAS:
773896-53-0
| Molecular Weight: | 398.41 g./mol | Molecular Formula: | C₁₈H₂₆N₂O₈ |
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| Density: | Storage Condition: | 2-8℃ |
Product Description:
Used primarily in organic synthesis, this compound serves as a key intermediate in the preparation of complex molecules, particularly in pharmaceutical research. Its structure is valuable for constructing heterocyclic frameworks, which are essential in developing drugs with therapeutic properties. The tert-butoxycarbonyl (Boc) groups provide protection for amine functionalities during multi-step synthetic processes, ensuring selective reactions. Additionally, the methoxycarbonyl groups enhance reactivity, facilitating further modifications. This chemical is often employed in the synthesis of biologically active compounds, including potential anticancer and antiviral agents, due to its ability to introduce specific functional groups into target molecules. Its application is crucial in medicinal chemistry for designing and optimizing drug candidates.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | $353.93 |
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N,N-bis-(tert-butoxycarbonyl)-2,5-bis-methoxycarbonyl-1,4-dihydropyrazine
Used primarily in organic synthesis, this compound serves as a key intermediate in the preparation of complex molecules, particularly in pharmaceutical research. Its structure is valuable for constructing heterocyclic frameworks, which are essential in developing drugs with therapeutic properties. The tert-butoxycarbonyl (Boc) groups provide protection for amine functionalities during multi-step synthetic processes, ensuring selective reactions. Additionally, the methoxycarbonyl groups enhance reactivity, facilitating further modifications. This chemical is often employed in the synthesis of biologically active compounds, including potential anticancer and antiviral agents, due to its ability to introduce specific functional groups into target molecules. Its application is crucial in medicinal chemistry for designing and optimizing drug candidates.
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