(S)-Methyl 2-amino-2-cyclopentylacetate hydrochloride
97%
- Product Code: 50317
CAS:
14328-62-2
| Molecular Weight: | 193.67 g./mol | Molecular Formula: | C₈H₁₆ClNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09800494 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of chiral drugs. Its structure, featuring a cyclopentyl group and an amino ester moiety, makes it a valuable building block for creating molecules with specific stereochemistry. It is often employed in the production of antiviral and anticancer agents, where precise chiral control is critical for efficacy and safety. Additionally, it serves as a key precursor in the preparation of peptidomimetics and other bioactive compounds, aiding in the exploration of new therapeutic targets. Its hydrochloride form enhances solubility, facilitating its use in various reaction conditions during organic synthesis.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿2,979.00 |
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| 1.000 | 10-20 days | ฿6,453.00 |
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| 5.000 | 10-20 days | ฿21,816.00 |
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| 10.000 | 10-20 days | ฿41,886.00 |
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(S)-Methyl 2-amino-2-cyclopentylacetate hydrochloride
This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of chiral drugs. Its structure, featuring a cyclopentyl group and an amino ester moiety, makes it a valuable building block for creating molecules with specific stereochemistry. It is often employed in the production of antiviral and anticancer agents, where precise chiral control is critical for efficacy and safety. Additionally, it serves as a key precursor in the preparation of peptidomimetics and other bioactive compounds, aiding in the exploration of new therapeutic targets. Its hydrochloride form enhances solubility, facilitating its use in various reaction conditions during organic synthesis.
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