Methyl 2-amino-3-(4-hydroxyphenyl)-2-methylpropanoate hydrochloride
≥95%
- Product Code: 50618
CAS:
7361-31-1
| Molecular Weight: | 245.70 g./mol | Molecular Formula: | C₁₁H₁₆ClNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00012606 | |
| Melting Point: | 192°C | Boiling Point: | 336.4°C at 760 mmHg |
| Density: | Storage Condition: | -20°C, store under inert gas |
Product Description:
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of drug intermediates. It serves as a key building block in the creation of compounds targeting neurological and cardiovascular disorders. Its structure is valuable for designing molecules that interact with specific receptors or enzymes in the body, aiding in the development of potential therapeutic agents. Additionally, it may be used in studies exploring anti-inflammatory or antioxidant properties due to its functional groups. Its hydrochloride form enhances solubility, making it suitable for various experimental and formulation processes in drug discovery.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Off-white to light yellow Solid |
| PURITY | 94.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿4,280.00 |
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| 0.250 | 10-20 days | ฿6,680.00 |
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| 1.000 | 10-20 days | ฿24,980.00 |
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Methyl 2-amino-3-(4-hydroxyphenyl)-2-methylpropanoate hydrochloride
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of drug intermediates. It serves as a key building block in the creation of compounds targeting neurological and cardiovascular disorders. Its structure is valuable for designing molecules that interact with specific receptors or enzymes in the body, aiding in the development of potential therapeutic agents. Additionally, it may be used in studies exploring anti-inflammatory or antioxidant properties due to its functional groups. Its hydrochloride form enhances solubility, making it suitable for various experimental and formulation processes in drug discovery.
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