Rel-(2R,3R)-1-(tert-Butoxycarbonyl)-3-cyclohexylpyrrolidine-2-carboxylic acid
95%
- Product Code: 54875
CAS:
1449586-26-8
| Molecular Weight: | 297.39 g./mol | Molecular Formula: | C₁₆H₂₇NO₄ |
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| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of complex organic compounds, particularly in the development of drugs targeting neurological and cardiovascular disorders. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a cyclohexyl moiety, makes it valuable for constructing peptidomimetics and other biologically active molecules. The compound is often employed in peptide coupling reactions, where its carboxylic acid group facilitates the formation of amide bonds, essential for creating peptide-based therapeutics. Additionally, its stereochemistry is crucial for ensuring the desired biological activity of the final drug product, making it a critical component in enantioselective synthesis processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.001 | 10-20 days | Ft34,326.31 |
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| 0.005 | 10-20 days | Ft95,609.43 |
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| 0.025 | 10-20 days | Ft318,827.40 |
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Rel-(2R,3R)-1-(tert-Butoxycarbonyl)-3-cyclohexylpyrrolidine-2-carboxylic acid
This chemical is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of complex organic compounds, particularly in the development of drugs targeting neurological and cardiovascular disorders. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a cyclohexyl moiety, makes it valuable for constructing peptidomimetics and other biologically active molecules. The compound is often employed in peptide coupling reactions, where its carboxylic acid group facilitates the formation of amide bonds, essential for creating peptide-based therapeutics. Additionally, its stereochemistry is crucial for ensuring the desired biological activity of the final drug product, making it a critical component in enantioselective synthesis processes.
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