5-(Chloromethyl)quinolin-8-ol hydrochloride
95%
- Product Code: 74521
CAS:
4053-45-6
| Molecular Weight: | 230.09 g./mol | Molecular Formula: | C₁₀H₉Cl₂NO |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 388.1°C | |
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in the synthesis of various pharmaceutical agents, particularly those targeting infectious diseases. Its structure serves as a key intermediate in the development of antimicrobial and antifungal drugs. Researchers also employ it in the preparation of quinoline derivatives, which are investigated for their potential therapeutic applications, including anti-inflammatory and anticancer properties. Additionally, it plays a role in organic synthesis, aiding in the creation of complex molecules for chemical research and drug discovery. Its versatility makes it valuable in medicinal chemistry and experimental pharmacology.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Yellow Solid |
| PURITY | 94.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿2,690.00 |
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| 1.000 | 10-20 days | ฿6,680.00 |
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| 5.000 | 10-20 days | ฿20,860.00 |
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5-(Chloromethyl)quinolin-8-ol hydrochloride
This compound is primarily utilized in the synthesis of various pharmaceutical agents, particularly those targeting infectious diseases. Its structure serves as a key intermediate in the development of antimicrobial and antifungal drugs. Researchers also employ it in the preparation of quinoline derivatives, which are investigated for their potential therapeutic applications, including anti-inflammatory and anticancer properties. Additionally, it plays a role in organic synthesis, aiding in the creation of complex molecules for chemical research and drug discovery. Its versatility makes it valuable in medicinal chemistry and experimental pharmacology.
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