Ethyl 6-fluoro-1-methyl-4-oxo-7-(piperazin-1-yl)-1,4-dihydro-[1,3]thiazeto[3,2-a]quinoline-3-carboxylate
≥95%
- Product Code: 120487
CAS:
113028-17-4
| Molecular Weight: | 377.43 g./mol | Molecular Formula: | C₁₈H₂₀FN₃O₃S |
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| EC Number: | MDL Number: | MFCD08063938 | |
| Melting Point: | Boiling Point: | 581.1°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of antibacterial agents. It plays a significant role in the development of fluoroquinolone derivatives, which are known for their broad-spectrum activity against various bacterial infections. The structural features of this compound, including the fluorine atom and the piperazine ring, contribute to its effectiveness in enhancing the potency and bioavailability of the resulting drugs. Researchers focus on modifying this compound to improve its pharmacological properties, such as increasing its antimicrobial activity and reducing potential side effects. It is particularly valuable in addressing resistant bacterial strains, making it a critical component in the ongoing fight against antibiotic resistance.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $13.56 |
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| 0.250 | 10-20 days | $23.05 |
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| 1.000 | 10-20 days | $79.11 |
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Ethyl 6-fluoro-1-methyl-4-oxo-7-(piperazin-1-yl)-1,4-dihydro-[1,3]thiazeto[3,2-a]quinoline-3-carboxylate
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of antibacterial agents. It plays a significant role in the development of fluoroquinolone derivatives, which are known for their broad-spectrum activity against various bacterial infections. The structural features of this compound, including the fluorine atom and the piperazine ring, contribute to its effectiveness in enhancing the potency and bioavailability of the resulting drugs. Researchers focus on modifying this compound to improve its pharmacological properties, such as increasing its antimicrobial activity and reducing potential side effects. It is particularly valuable in addressing resistant bacterial strains, making it a critical component in the ongoing fight against antibiotic resistance.
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