2-AMINO-3-(1,2-DIHYDRO-2-OXOQUINOLINE-4-YL)PROPANOIC ACID HYDROCHLORIDE
98%
- Product Code: 73320
Alias:
Related CAS: 5162-90-3
CAS:
132210-24-3
| Molecular Weight: | 268.7?anhy? g./mol | Molecular Formula: | C₁₂H₁₃ClN₂O₃ |
|---|---|---|---|
| EC Number: | 1312995-182-4 | MDL Number: | |
| Melting Point: | 220-221 ºC | Boiling Point: | 522.716 ºC at 760 mmHg |
| Density: | 1.344 g/cm3 | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of pharmaceutical research and development. It serves as a key intermediate in the synthesis of various bioactive molecules, particularly those targeting neurological and inflammatory conditions. Its unique structure allows it to act as a precursor in the creation of quinoline derivatives, which are known for their therapeutic potential. Researchers often employ it in the design and optimization of drug candidates, focusing on enhancing efficacy and reducing side effects. Additionally, it is explored in studies related to enzyme inhibition and receptor modulation, contributing to advancements in medicinal chemistry.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | solid |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | ฿1,040.00 |
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| 25.000 | 10-20 days | ฿2,690.00 |
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| 100.000 | 10-20 days | ฿8,010.00 |
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| 500.000 | 10-20 days | ฿24,930.00 |
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2-AMINO-3-(1,2-DIHYDRO-2-OXOQUINOLINE-4-YL)PROPANOIC ACID HYDROCHLORIDE
This compound is primarily utilized in the field of pharmaceutical research and development. It serves as a key intermediate in the synthesis of various bioactive molecules, particularly those targeting neurological and inflammatory conditions. Its unique structure allows it to act as a precursor in the creation of quinoline derivatives, which are known for their therapeutic potential. Researchers often employ it in the design and optimization of drug candidates, focusing on enhancing efficacy and reducing side effects. Additionally, it is explored in studies related to enzyme inhibition and receptor modulation, contributing to advancements in medicinal chemistry.
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