(S)-2-Amino-3-(4-(prop-2-yn-1-yloxy)phenyl)propanoic acid
95%
- Product Code: 78489
CAS:
610794-20-2
| Molecular Weight: | 219.24 g./mol | Molecular Formula: | C₁₂H₁₃NO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD21363200 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry, airtight |
Product Description:
This compound is primarily explored in the field of medicinal chemistry for its potential as a building block in the synthesis of biologically active molecules. Its structure, featuring an amino acid backbone and a propargyl ether group, makes it a versatile intermediate for developing enzyme inhibitors or receptor modulators. It is particularly useful in designing compounds targeting neurological disorders or inflammation due to its ability to interact with specific biological pathways. Additionally, the alkyne group allows for further functionalization via click chemistry, enabling the creation of complex molecules for drug discovery or biochemical studies. Its applications extend to research in peptide-based therapeutics and as a probe in studying protein interactions.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿7,362.00 |
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| 0.250 | 10-20 days | ฿11,043.00 |
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| 1.000 | 10-20 days | ฿28,710.00 |
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(S)-2-Amino-3-(4-(prop-2-yn-1-yloxy)phenyl)propanoic acid
This compound is primarily explored in the field of medicinal chemistry for its potential as a building block in the synthesis of biologically active molecules. Its structure, featuring an amino acid backbone and a propargyl ether group, makes it a versatile intermediate for developing enzyme inhibitors or receptor modulators. It is particularly useful in designing compounds targeting neurological disorders or inflammation due to its ability to interact with specific biological pathways. Additionally, the alkyne group allows for further functionalization via click chemistry, enabling the creation of complex molecules for drug discovery or biochemical studies. Its applications extend to research in peptide-based therapeutics and as a probe in studying protein interactions.
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