(S)-3-((tert-Butoxycarbonyl)amino)-3-(2,3-dichlorophenyl)propanoic acid
98%
- Product Code: 233325
CAS:
499995-82-3
| Molecular Weight: | 334.2 g./mol | Molecular Formula: | C₁₄H₁₇Cl₂NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03427905 | |
| Melting Point: | Boiling Point: | 468.9±45.0 °C(Predicted) | |
| Density: | 1.321±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
Used as a key chiral intermediate in the synthesis of angiotensin II receptor antagonists, particularly in the production of antihypertensive drugs like valsartan and related sartan-class medications. Its stereochemistry enables selective binding and improved pharmacokinetic properties in the final drug substance. The Boc-protected amine and carboxylic acid functional groups allow for stepwise peptide-like coupling and deprotection strategies in multi-step organic synthesis. Commonly employed in pharmaceutical research and development for building complex molecules requiring high enantiomeric purity.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿5,060.00 |
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| 250mg | 10-20 days | ฿8,600.00 |
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(S)-3-((tert-Butoxycarbonyl)amino)-3-(2,3-dichlorophenyl)propanoic acid
Used as a key chiral intermediate in the synthesis of angiotensin II receptor antagonists, particularly in the production of antihypertensive drugs like valsartan and related sartan-class medications. Its stereochemistry enables selective binding and improved pharmacokinetic properties in the final drug substance. The Boc-protected amine and carboxylic acid functional groups allow for stepwise peptide-like coupling and deprotection strategies in multi-step organic synthesis. Commonly employed in pharmaceutical research and development for building complex molecules requiring high enantiomeric purity.
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