(3R,4S,5S)-4-[[(1,1-Dimethylethoxy)carbonyl]methylamino]-3-methoxy-5-methylheptanoic acid
≥95%
- Product Code: 70906
CAS:
132149-81-6
| Molecular Weight: | 303.39 g./mol | Molecular Formula: | C₁₅H₂₉NO₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD23381192 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C, dry, sealed |
Product Description:
This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of complex drug molecules. Its unique structure, featuring multiple functional groups, makes it valuable for constructing specific pharmacophores in medicinal chemistry. It is often employed in the development of protease inhibitors, particularly those targeting enzymes involved in viral replication or other disease pathways. The compound's stereochemistry and functional groups allow for precise interactions with biological targets, enhancing the efficacy and selectivity of the resulting drugs. Additionally, it serves as a building block in the production of peptide-based therapeutics, where its chiral centers and protective groups are crucial for achieving the desired biological activity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿33,282.00 |
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| 0.250 | 10-20 days | ฿62,982.00 |
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(3R,4S,5S)-4-[[(1,1-Dimethylethoxy)carbonyl]methylamino]-3-methoxy-5-methylheptanoic acid
This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of complex drug molecules. Its unique structure, featuring multiple functional groups, makes it valuable for constructing specific pharmacophores in medicinal chemistry. It is often employed in the development of protease inhibitors, particularly those targeting enzymes involved in viral replication or other disease pathways. The compound's stereochemistry and functional groups allow for precise interactions with biological targets, enhancing the efficacy and selectivity of the resulting drugs. Additionally, it serves as a building block in the production of peptide-based therapeutics, where its chiral centers and protective groups are crucial for achieving the desired biological activity.
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