(R)-2-Amino-3-(phenylthio)propanoic acid
97%
- Product Code: 55892
CAS:
34317-61-8
| Molecular Weight: | 197.25 g./mol | Molecular Formula: | C₉H₁₁NO₂S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01318758 | |
| Melting Point: | 200°C (dec.) | Boiling Point: | 361.5°C at 760 mmHg |
| Density: | Storage Condition: | Room temperature, away from light, stored in an inert gas |
Product Description:
This compound is primarily utilized in the field of organic synthesis, where it serves as a chiral building block for the creation of complex molecules. Its structure, featuring both an amino group and a phenylthio group, makes it valuable in the development of pharmaceuticals, particularly in the synthesis of enantiomerically pure drugs. It is often employed in peptide chemistry to introduce specific functional groups or to modify peptide chains, enhancing their biological activity or stability. Additionally, it finds application in asymmetric synthesis, aiding in the production of compounds with high stereochemical purity, which is crucial in the development of active pharmaceutical ingredients (APIs) and fine chemicals.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to off-white powder |
| PURITY | 96.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿270.00 |
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| 0.250 | 10-20 days | ฿370.00 |
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| 1.000 | 10-20 days | ฿770.00 |
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| 5.000 | 10-20 days | ฿2,690.00 |
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(R)-2-Amino-3-(phenylthio)propanoic acid
This compound is primarily utilized in the field of organic synthesis, where it serves as a chiral building block for the creation of complex molecules. Its structure, featuring both an amino group and a phenylthio group, makes it valuable in the development of pharmaceuticals, particularly in the synthesis of enantiomerically pure drugs. It is often employed in peptide chemistry to introduce specific functional groups or to modify peptide chains, enhancing their biological activity or stability. Additionally, it finds application in asymmetric synthesis, aiding in the production of compounds with high stereochemical purity, which is crucial in the development of active pharmaceutical ingredients (APIs) and fine chemicals.
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