(S)-2-((tert-Butoxycarbonyl)amino)-3-(3-chloro-4-fluorophenyl)propanoic acid
98%
- Product Code: 236418
CAS:
1629658-18-9
| Molecular Weight: | 317.744 g./mol | Molecular Formula: | C₁₄H₁₇ClFNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD31707241 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, seal, dry |
Product Description:
Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of angiotensin II receptor antagonists for the treatment of hypertension. Its stereochemistry enables selective interactions in drug molecules, enhancing efficacy and reducing side effects. Commonly employed in peptide coupling reactions due to the protected amine group, allowing stepwise construction of complex bioactive molecules. The presence of halogen substituents facilitates further functionalization through cross-coupling reactions, expanding its utility in medicinal chemistry.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿12,140.00 |
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| 1g | 10-20 days | ฿49,100.00 |
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| 250mg | 10-20 days | ฿18,180.00 |
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(S)-2-((tert-Butoxycarbonyl)amino)-3-(3-chloro-4-fluorophenyl)propanoic acid
Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of angiotensin II receptor antagonists for the treatment of hypertension. Its stereochemistry enables selective interactions in drug molecules, enhancing efficacy and reducing side effects. Commonly employed in peptide coupling reactions due to the protected amine group, allowing stepwise construction of complex bioactive molecules. The presence of halogen substituents facilitates further functionalization through cross-coupling reactions, expanding its utility in medicinal chemistry.
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