(R)-Ethyl 5-([1,1'-biphenyl]-4-yl)-4-((tert-butoxycarbonyl)amino)-2-methylpent-2-enoate
97%
- Product Code: 230443
CAS:
149709-59-1
| Molecular Weight: | 409.52 g./mol | Molecular Formula: | C₂₅H₃₁NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD23378892 | |
| Melting Point: | Boiling Point: | 562.7±50.0°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry seal |
Product Description:
Used as a key chiral intermediate in the synthesis of protease inhibitors, particularly in the development of antiviral agents such as hepatitis C virus (HCV) inhibitors. Its stereochemistry enables selective binding to enzyme active sites, enhancing drug efficacy. The tert-butoxycarbonyl (Boc) protecting group facilitates stepwise peptide coupling, while the ester moiety allows for further functionalization. Commonly employed in multi-step organic syntheses where enantiomeric purity is critical for biological activity.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿180.00 |
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| 250mg | 10-20 days | ฿340.00 |
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| 1g | 10-20 days | ฿1,120.00 |
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| 5g | 10-20 days | ฿3,880.00 |
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| 25g | 10-20 days | ฿16,980.00 |
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(R)-Ethyl 5-([1,1'-biphenyl]-4-yl)-4-((tert-butoxycarbonyl)amino)-2-methylpent-2-enoate
Used as a key chiral intermediate in the synthesis of protease inhibitors, particularly in the development of antiviral agents such as hepatitis C virus (HCV) inhibitors. Its stereochemistry enables selective binding to enzyme active sites, enhancing drug efficacy. The tert-butoxycarbonyl (Boc) protecting group facilitates stepwise peptide coupling, while the ester moiety allows for further functionalization. Commonly employed in multi-step organic syntheses where enantiomeric purity is critical for biological activity.
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