(S)-Methyl 3-amino-3-(2-methoxyphenyl)propanoate hydrochloride
97%
- Product Code: 38435
CAS:
1391398-83-6
| Molecular Weight: | 245.70 g./mol | Molecular Formula: | C₁₁H₁₆ClNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD12911028 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of chiral molecules. Its structure, featuring an amino group and a methoxyphenyl moiety, makes it a valuable intermediate in the production of active pharmaceutical ingredients (APIs) that target neurological and psychiatric disorders. It is often employed in the creation of compounds that interact with neurotransmitter systems, such as serotonin and dopamine receptors, due to its potential to modulate these pathways. Additionally, its chiral nature allows for the development of enantiomerically pure drugs, enhancing efficacy and reducing side effects in therapeutic applications. Researchers also explore its use in asymmetric synthesis, where it serves as a building block for complex organic molecules with high stereochemical precision.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿10,368.00 |
+
-
|
| 0.250 | 10-20 days | ฿20,745.00 |
+
-
|
(S)-Methyl 3-amino-3-(2-methoxyphenyl)propanoate hydrochloride
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of chiral molecules. Its structure, featuring an amino group and a methoxyphenyl moiety, makes it a valuable intermediate in the production of active pharmaceutical ingredients (APIs) that target neurological and psychiatric disorders. It is often employed in the creation of compounds that interact with neurotransmitter systems, such as serotonin and dopamine receptors, due to its potential to modulate these pathways. Additionally, its chiral nature allows for the development of enantiomerically pure drugs, enhancing efficacy and reducing side effects in therapeutic applications. Researchers also explore its use in asymmetric synthesis, where it serves as a building block for complex organic molecules with high stereochemical precision.
| Mechanism | - |
| Appearance | - |
| Longevity | - |
| Strength | - |
| Storage | - |
| Shelf Life | - |
| Allergen(s) | - |
| Dosage (Range) | - |
| Recommended Dosage | - |
| Dosage (Per Day) | - |
| Recommended Dosage (Per Day) | - |
| Mix Method | - |
| Heat Resistance | - |
| Stable in pH range | - |
| Solubility | - |
| Product Types | - |
| INCI | - |
Cart
No products
Subtotal:
฿0.00
฿0.00
Total :