(R)-2-Amino-4-cyclohexylbutanoic acid
97%
- Product Code: 55873
CAS:
728880-26-0
| Molecular Weight: | 185.26 g./mol | Molecular Formula: | C₁₀H₁₉NO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18252743 | |
| Melting Point: | Boiling Point: | 321.4±25.0°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 pharmaceutical research and development. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting neurological and metabolic disorders. Its structural properties make it valuable for designing peptide-based drugs, where its chiral center and cyclohexyl group contribute to enhanced binding affinity and stability. Additionally, it is explored in the creation of enzyme inhibitors and receptor modulators, aiding in the study of disease mechanisms and potential therapeutic interventions. Its applications also extend to organic synthesis, where it is used to construct complex molecules with specific stereochemical configurations.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿666.00 |
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| 1.000 | 10-20 days | ฿1,953.00 |
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| 5.000 | 10-20 days | ฿4,473.00 |
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(R)-2-Amino-4-cyclohexylbutanoic acid
This compound is primarily utilized in the field of pharmaceutical research and development. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting neurological and metabolic disorders. Its structural properties make it valuable for designing peptide-based drugs, where its chiral center and cyclohexyl group contribute to enhanced binding affinity and stability. Additionally, it is explored in the creation of enzyme inhibitors and receptor modulators, aiding in the study of disease mechanisms and potential therapeutic interventions. Its applications also extend to organic synthesis, where it is used to construct complex molecules with specific stereochemical configurations.
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