(R)-3-Amino-3-phenylpropanoic acid hydrochloride
97%
- Product Code: 37613
CAS:
83649-48-3
| Molecular Weight: | 201.65 g./mol | Molecular Formula: | C₉H₁₂ClNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01076237 | |
| Melting Point: | Boiling Point: | 307.5°C at 760 mmHg | |
| Density: | Storage Condition: | room temperature, stored under inert gas |
Product Description:
This compound is primarily utilized in the pharmaceutical industry as a chiral building block for the synthesis of various drugs. Its structure, featuring both an amino group and a phenyl ring, makes it valuable in the production of active pharmaceutical ingredients (APIs) that target neurological and psychiatric disorders. It is often employed in the development of compounds that interact with neurotransmitter systems, such as GABA analogs, which are used in treating conditions like epilepsy, anxiety, and chronic pain. Additionally, its enantiomeric purity is crucial for ensuring the efficacy and safety of the resulting drugs, as the (R)-configuration can lead to specific biological activity. Beyond pharmaceuticals, it may also serve as an intermediate in organic synthesis for creating complex molecules with potential therapeutic applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿828.00 |
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| 1.000 | 10-20 days | ฿2,061.00 |
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| 5.000 | 10-20 days | ฿6,579.00 |
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| 10.000 | 10-20 days | ฿11,178.00 |
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(R)-3-Amino-3-phenylpropanoic acid hydrochloride
This compound is primarily utilized in the pharmaceutical industry as a chiral building block for the synthesis of various drugs. Its structure, featuring both an amino group and a phenyl ring, makes it valuable in the production of active pharmaceutical ingredients (APIs) that target neurological and psychiatric disorders. It is often employed in the development of compounds that interact with neurotransmitter systems, such as GABA analogs, which are used in treating conditions like epilepsy, anxiety, and chronic pain. Additionally, its enantiomeric purity is crucial for ensuring the efficacy and safety of the resulting drugs, as the (R)-configuration can lead to specific biological activity. Beyond pharmaceuticals, it may also serve as an intermediate in organic synthesis for creating complex molecules with potential therapeutic applications.
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