4-Chloro-7-fluoroquinoline
≥95%
Reagent
Code: #119169
CAS Number
391-82-2
blur_circular Chemical Specifications
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Molecular Information
Weight
181.59 g/mol
Formula
C₉H₅ClFN
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Registry Numbers
MDL Number
MFCD00153094
thermostat
Physical Properties
Boiling Point
259.9±20.0°C at 760 mmHg
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Storage & Handling
Storage
2-8°C, store under inert gas
description Product Description
4-Chloro-7-fluoroquinoline is primarily used in pharmaceutical research and development as a key intermediate in the synthesis of various biologically active compounds. Its structure is particularly valuable in the creation of quinolone-based antibiotics, which are widely used to treat bacterial infections. The compound’s unique halogenated quinolone core allows for modifications that enhance the efficacy and specificity of antimicrobial agents. Additionally, it serves as a building block in the development of other therapeutic agents, including anticancer and anti-inflammatory drugs, due to its ability to interact with biological targets. In medicinal chemistry, it is also employed to study structure-activity relationships, aiding in the optimization of drug candidates for improved potency and reduced side effects. Beyond pharmaceuticals, it finds limited use in organic synthesis for constructing complex heterocyclic frameworks.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Appearance | White to Yellow Solid |
Purity (%) | 94.5-100% |
Infrared Spectrum | Conforms To Structure |
NMR | Conforms To Structure |
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4-Chloro-7-fluoroquinoline
4-Chloro-7-fluoroquinoline is primarily used in pharmaceutical research and development as a key intermediate in the synthesis of various biologically active compounds. Its structure is particularly valuable in the creation of quinolone-based antibiotics, which are widely used to treat bacterial infections. The compound’s unique halogenated quinolone core allows for modifications that enhance the efficacy and specificity of antimicrobial agents. Additionally, it serves as a building block in the development of other therapeutic agents, including anticancer and anti-inflammatory drugs, due to its ability to interact with biological targets. In medicinal chemistry, it is also employed to study structure-activity relationships, aiding in the optimization of drug candidates for improved potency and reduced side effects. Beyond pharmaceuticals, it finds limited use in organic synthesis for constructing complex heterocyclic frameworks.
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