tert-Butyl6-((tert-Butoxycarbonyl)amino)-3-oxo-3,4-dihydroquinoxaline-1(2H)-carboxylate
≥95%
- Product Code: 57057
CAS:
959246-52-7
| Molecular Weight: | 363.41 g./mol | Molecular Formula: | C₁₈H₂₅N₃O₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09878781 | |
| Melting Point: | Boiling Point: | 476.9 °C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
This chemical is primarily utilized in organic synthesis as a key intermediate in the preparation of more complex molecules. It is often employed in the development of pharmaceuticals, particularly in the synthesis of compounds with potential therapeutic applications. The presence of the tert-butoxycarbonyl (Boc) protecting group makes it valuable in peptide synthesis, where it safeguards amino groups during reactions. Additionally, its structure is useful in the creation of quinoxaline derivatives, which are explored for their biological activities, including antimicrobial, anticancer, and anti-inflammatory properties. Its role in facilitating controlled and selective reactions makes it a critical component in medicinal chemistry and drug discovery processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $147.94 |
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| 0.250 | 10-20 days | $262.06 |
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tert-Butyl6-((tert-Butoxycarbonyl)amino)-3-oxo-3,4-dihydroquinoxaline-1(2H)-carboxylate
This chemical is primarily utilized in organic synthesis as a key intermediate in the preparation of more complex molecules. It is often employed in the development of pharmaceuticals, particularly in the synthesis of compounds with potential therapeutic applications. The presence of the tert-butoxycarbonyl (Boc) protecting group makes it valuable in peptide synthesis, where it safeguards amino groups during reactions. Additionally, its structure is useful in the creation of quinoxaline derivatives, which are explored for their biological activities, including antimicrobial, anticancer, and anti-inflammatory properties. Its role in facilitating controlled and selective reactions makes it a critical component in medicinal chemistry and drug discovery processes.
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