(1S,3R,4R)-Ethyl 3-((tert-butoxycarbonyl)amino)-4-hydroxycyclohexanecarboxylate
97%
- Product Code: 70841
CAS:
365997-33-7
| Molecular Weight: | 287.35 g./mol | Molecular Formula: | C₁₄H₂₅NO₅ |
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| EC Number: | MDL Number: | MFCD23106245 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dry, sealed |
Product Description:
This compound is primarily utilized in the synthesis of complex organic molecules, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of various bioactive compounds and drug candidates. Its structure, featuring both hydroxyl and tert-butoxycarbonyl-protected amino groups, makes it valuable for constructing chiral centers in medicinal chemistry. It is often employed in the development of peptidomimetics and other therapeutic agents targeting specific biological pathways. Additionally, its stereochemistry is leveraged in asymmetric synthesis to achieve high enantiomeric purity in final products.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 5.000 | 10-20 days | $85.22 |
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| 25.000 | 10-20 days | $276.58 |
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| 100.000 | 10-20 days | $515.42 |
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(1S,3R,4R)-Ethyl 3-((tert-butoxycarbonyl)amino)-4-hydroxycyclohexanecarboxylate
This compound is primarily utilized in the synthesis of complex organic molecules, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of various bioactive compounds and drug candidates. Its structure, featuring both hydroxyl and tert-butoxycarbonyl-protected amino groups, makes it valuable for constructing chiral centers in medicinal chemistry. It is often employed in the development of peptidomimetics and other therapeutic agents targeting specific biological pathways. Additionally, its stereochemistry is leveraged in asymmetric synthesis to achieve high enantiomeric purity in final products.
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