2-Amino-4-methoxy-4-oxobutanoic acid hydrochloride
97%
- Product Code: 53381
CAS:
1835-52-5
| Molecular Weight: | 183.59 g./mol | Molecular Formula: | C₅H₁₀ClNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00214167 | |
| Melting Point: | Boiling Point: | 305°C at 760 mmHg | |
| Density: | Storage Condition: | -20°C, store under inert gas |
Product Description:
This compound is primarily used in biochemical research and pharmaceutical development. It serves as a key intermediate in the synthesis of various bioactive molecules, particularly those targeting neurological and metabolic pathways. Its structure allows it to participate in peptide synthesis, making it valuable in creating modified peptides for therapeutic applications. Additionally, it is utilized in studies exploring enzyme mechanisms and protein interactions due to its ability to mimic natural amino acids. In drug discovery, it aids in developing compounds with potential anti-inflammatory or neuroprotective properties. Its hydrochloride form enhances solubility, facilitating its use in experimental and industrial processes.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to yellow powder or crystals |
| PURITY | 96.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | £19.22 |
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| 1.000 | 10-20 days | £38.45 |
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2-Amino-4-methoxy-4-oxobutanoic acid hydrochloride
This compound is primarily used in biochemical research and pharmaceutical development. It serves as a key intermediate in the synthesis of various bioactive molecules, particularly those targeting neurological and metabolic pathways. Its structure allows it to participate in peptide synthesis, making it valuable in creating modified peptides for therapeutic applications. Additionally, it is utilized in studies exploring enzyme mechanisms and protein interactions due to its ability to mimic natural amino acids. In drug discovery, it aids in developing compounds with potential anti-inflammatory or neuroprotective properties. Its hydrochloride form enhances solubility, facilitating its use in experimental and industrial processes.
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