Ethyl 7-chloro-4-hydroxyquinoline-3-carboxylate

95%

Reagent Code: #184317
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CAS Number 16600-22-9

science Other reagents with same CAS 16600-22-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 251.67 g/mol
Formula C₁₂H₁₀ClNO₃
badge Registry Numbers
MDL Number MFCD00438741
thermostat Physical Properties
Boiling Point 378.4 °C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

Used as an intermediate in the synthesis of quinolone antibiotics, particularly in the production of fluoroquinolone drugs which exhibit broad-spectrum antibacterial activity. Its structure serves as a core scaffold for building active pharmaceutical ingredients targeting DNA gyrase and topoisomerase IV in bacteria. Commonly employed in medicinal chemistry research for developing new anti-infective agents with improved potency and reduced resistance. Also utilized in the preparation of fluorescent probes due to the inherent photophysical properties of the quinoline ring system, enabling applications in bioimaging and molecular sensing.

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inventory 1g
10-20 days ฿22,430.00

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Ethyl 7-chloro-4-hydroxyquinoline-3-carboxylate
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Used as an intermediate in the synthesis of quinolone antibiotics, particularly in the production of fluoroquinolone drugs which exhibit broad-spectrum antibacterial activity. Its structure serves as a core scaffold for building active pharmaceutical ingredients targeting DNA gyrase and topoisomerase IV in bacteria. Commonly employed in medicinal chemistry research for developing new anti-infective agents with improved potency and reduced resistance. Also utilized in the preparation of fluorescent probes

Used as an intermediate in the synthesis of quinolone antibiotics, particularly in the production of fluoroquinolone drugs which exhibit broad-spectrum antibacterial activity. Its structure serves as a core scaffold for building active pharmaceutical ingredients targeting DNA gyrase and topoisomerase IV in bacteria. Commonly employed in medicinal chemistry research for developing new anti-infective agents with improved potency and reduced resistance. Also utilized in the preparation of fluorescent probes due to the inherent photophysical properties of the quinoline ring system, enabling applications in bioimaging and molecular sensing.

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