(1R,3R)-3-(((Benzyloxy)carbonyl)amino)cyclohexyl acetate
95%
- Product Code: 87026
CAS:
750649-42-4
| Molecular Weight: | 291.34 g./mol | Molecular Formula: | C₁₆H₂₁NO₄ |
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| EC Number: | MDL Number: | MFCD30472098 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry, airtight |
Product Description:
This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs) for therapeutic drugs. Its structure, featuring a benzyloxycarbonyl-protected amine and an acetate group, makes it a valuable building block in organic synthesis. It is often employed in the preparation of cyclohexane-based compounds, which are key components in drugs targeting neurological and inflammatory conditions. Additionally, it serves as a precursor in the production of chiral molecules, enabling the creation of enantiomerically pure substances critical for drug efficacy and safety. Its role in peptide synthesis is also notable, as it aids in the protection and deprotection of amino groups during the formation of complex peptide chains.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿12,825.00 |
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(1R,3R)-3-(((Benzyloxy)carbonyl)amino)cyclohexyl acetate
This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs) for therapeutic drugs. Its structure, featuring a benzyloxycarbonyl-protected amine and an acetate group, makes it a valuable building block in organic synthesis. It is often employed in the preparation of cyclohexane-based compounds, which are key components in drugs targeting neurological and inflammatory conditions. Additionally, it serves as a precursor in the production of chiral molecules, enabling the creation of enantiomerically pure substances critical for drug efficacy and safety. Its role in peptide synthesis is also notable, as it aids in the protection and deprotection of amino groups during the formation of complex peptide chains.
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