(2R,3S)-2-Amino-3-hydroxy-4-methylpentanoic acid
97%
- Product Code: 55094
CAS:
87421-23-6
| Molecular Weight: | 147.17 g./mol | Molecular Formula: | C₆H₁₃NO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00142970 | |
| Melting Point: | 205-208°C | Boiling Point: | 319°C at 760 mmHg |
| Density: | Storage Condition: | Room temperature, away from light, stored in an inert gas |
Product Description:
This compound is primarily used in the synthesis of specialized peptides and proteins, where its unique structure allows it to act as a building block for creating specific molecular configurations. It is particularly valuable in the development of enzyme inhibitors, which can be used in biochemical research to study enzyme functions and pathways. Additionally, it finds application in the pharmaceutical industry for the design of drugs that target specific biological processes, such as those involved in metabolic disorders or infections. Its stereochemistry also makes it useful in asymmetric synthesis, enabling the production of chiral molecules with high precision.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | £480.39 |
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| 0.250 | 10-20 days | £952.63 |
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(2R,3S)-2-Amino-3-hydroxy-4-methylpentanoic acid
This compound is primarily used in the synthesis of specialized peptides and proteins, where its unique structure allows it to act as a building block for creating specific molecular configurations. It is particularly valuable in the development of enzyme inhibitors, which can be used in biochemical research to study enzyme functions and pathways. Additionally, it finds application in the pharmaceutical industry for the design of drugs that target specific biological processes, such as those involved in metabolic disorders or infections. Its stereochemistry also makes it useful in asymmetric synthesis, enabling the production of chiral molecules with high precision.
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