(S)-3-Amino-3-cyclohexylpropanoic acid
95%
- Product Code: 57170
CAS:
91383-14-1
| Molecular Weight: | 171.24 g./mol | Molecular Formula: | C₉H₁₇NO₂ |
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| EC Number: | MDL Number: | MFCD07373036 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
(S)-3-Amino-3-cyclohexylpropanoic acid is primarily used in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of various pharmaceutical compounds, particularly those targeting neurological and metabolic disorders. Its structure allows it to act as a building block for designing molecules that can interact with specific biological targets, such as enzymes or receptors.
In research, it is often employed to develop peptide analogs and other bioactive molecules due to its chiral center, which can influence the stereochemistry and efficacy of the final drug. Additionally, it has been explored in the creation of inhibitors for enzymes involved in disease pathways, making it valuable for therapeutic applications. Its cyclohexyl group contributes to the stability and lipophilicity of the resulting compounds, enhancing their potential as drug candidates.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | Ft17,551.02 |
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| 0.250 | 10-20 days | Ft26,278.05 |
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| 1.000 | 10-20 days | Ft74,470.63 |
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(S)-3-Amino-3-cyclohexylpropanoic acid
(S)-3-Amino-3-cyclohexylpropanoic acid is primarily used in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of various pharmaceutical compounds, particularly those targeting neurological and metabolic disorders. Its structure allows it to act as a building block for designing molecules that can interact with specific biological targets, such as enzymes or receptors.
In research, it is often employed to develop peptide analogs and other bioactive molecules due to its chiral center, which can influence the stereochemistry and efficacy of the final drug. Additionally, it has been explored in the creation of inhibitors for enzymes involved in disease pathways, making it valuable for therapeutic applications. Its cyclohexyl group contributes to the stability and lipophilicity of the resulting compounds, enhancing their potential as drug candidates.
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