(2R)-2-amino-3-(propylsulfinyl)propanoic acid
95%
- Product Code: 87061
CAS:
17795-24-3
| Molecular Weight: | 179.24 g./mol | Molecular Formula: | C₆H₁₃NO₃S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03093729 | |
| Melting Point: | Boiling Point: | 412.7 °C at 760 mmHg | |
| Density: | 1.32 g/cm3(Predicted) | Storage Condition: | room temperature, inert atmosphere |
Product Description:
This compound is primarily utilized in the field of biochemistry and pharmacology due to its unique structure and properties. It serves as a precursor or intermediate in the synthesis of more complex molecules, particularly those involved in drug development. Its sulfinyl group makes it a valuable component in the creation of compounds that target specific enzymes or receptors in biological systems.
In research, it is often employed to study the mechanisms of enzyme inhibition and to explore its potential as a therapeutic agent. Its chiral nature allows for the investigation of stereoselective reactions, which is crucial in the design of drugs with high specificity and reduced side effects. Additionally, it may be used in the development of prodrugs, where its properties can enhance the bioavailability or stability of active pharmaceutical ingredients.
Overall, this chemical plays a significant role in advancing medicinal chemistry and understanding biochemical pathways.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿5,400.00 |
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| 0.250 | 10-20 days | ฿10,800.00 |
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| 1.000 | 10-20 days | ฿21,600.00 |
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(2R)-2-amino-3-(propylsulfinyl)propanoic acid
This compound is primarily utilized in the field of biochemistry and pharmacology due to its unique structure and properties. It serves as a precursor or intermediate in the synthesis of more complex molecules, particularly those involved in drug development. Its sulfinyl group makes it a valuable component in the creation of compounds that target specific enzymes or receptors in biological systems.
In research, it is often employed to study the mechanisms of enzyme inhibition and to explore its potential as a therapeutic agent. Its chiral nature allows for the investigation of stereoselective reactions, which is crucial in the design of drugs with high specificity and reduced side effects. Additionally, it may be used in the development of prodrugs, where its properties can enhance the bioavailability or stability of active pharmaceutical ingredients.
Overall, this chemical plays a significant role in advancing medicinal chemistry and understanding biochemical pathways.
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