(S)-3-((tert-Butoxycarbonyl)amino)-3-(2,4-dichlorophenyl)propanoic acid
97%
- Product Code: 50503
CAS:
499995-81-2
| Molecular Weight: | 334.20 g./mol | Molecular Formula: | C₁₄H₁₇Cl₂NO₄ |
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| EC Number: | MDL Number: | MFCD03427904 | |
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| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This compound is primarily used in the synthesis of pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs). Its structure, featuring a Boc-protected amino group and a dichlorophenyl moiety, makes it a valuable building block in the production of complex molecules, especially those targeting therapeutic areas such as central nervous system disorders, infections, or inflammatory diseases. It is often employed in peptide coupling reactions or as a precursor in the synthesis of chiral compounds, leveraging its stereochemistry for the creation of enantiomerically pure drugs. Additionally, its dichlorophenyl group can contribute to the biological activity of the final drug molecule, making it a key component in medicinal chemistry research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $27.05 |
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| 0.250 | 10-20 days | $58.75 |
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(S)-3-((tert-Butoxycarbonyl)amino)-3-(2,4-dichlorophenyl)propanoic acid
This compound is primarily used in the synthesis of pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs). Its structure, featuring a Boc-protected amino group and a dichlorophenyl moiety, makes it a valuable building block in the production of complex molecules, especially those targeting therapeutic areas such as central nervous system disorders, infections, or inflammatory diseases. It is often employed in peptide coupling reactions or as a precursor in the synthesis of chiral compounds, leveraging its stereochemistry for the creation of enantiomerically pure drugs. Additionally, its dichlorophenyl group can contribute to the biological activity of the final drug molecule, making it a key component in medicinal chemistry research.
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