tert-Butyl 3-((di-tert-butoxycarbonyl)amino)-5-(1-hydroxyethyl)-1H-pyrazole-1-carboxylate
95%
- Product Code: 44165
CAS:
1439824-04-0
| Molecular Weight: | 427.4919 g./mol | Molecular Formula: | C₂₀H₃₃N₃O₇ |
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| EC Number: | MDL Number: | MFCD22690763 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily used in organic synthesis as a protected intermediate for the development of more complex molecules, particularly in pharmaceutical research. Its structure, featuring multiple tert-butoxycarbonyl (Boc) groups, allows it to act as a protective agent for amino and hydroxyl functionalities during chemical reactions. This ensures that these sensitive groups remain intact while other parts of the molecule undergo transformations. It is often employed in the synthesis of pyrazole derivatives, which are valuable in drug discovery for their potential biological activities, such as anti-inflammatory, antimicrobial, or anticancer properties. Additionally, its stability and ease of deprotection make it a preferred choice in multi-step synthetic processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | Ft88,239.94 |
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tert-Butyl 3-((di-tert-butoxycarbonyl)amino)-5-(1-hydroxyethyl)-1H-pyrazole-1-carboxylate
This compound is primarily used in organic synthesis as a protected intermediate for the development of more complex molecules, particularly in pharmaceutical research. Its structure, featuring multiple tert-butoxycarbonyl (Boc) groups, allows it to act as a protective agent for amino and hydroxyl functionalities during chemical reactions. This ensures that these sensitive groups remain intact while other parts of the molecule undergo transformations. It is often employed in the synthesis of pyrazole derivatives, which are valuable in drug discovery for their potential biological activities, such as anti-inflammatory, antimicrobial, or anticancer properties. Additionally, its stability and ease of deprotection make it a preferred choice in multi-step synthetic processes.
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