5-Chloro-8-hydroxy-7-iodoquinoline

98.0%

Reagent Code: #120038
label
Alias 5-Chloro-7-iodo-8-hydroxyquinoline; Clioquinol; Clioquinol; Quino imitation
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CAS Number 130-26-7

science Other reagents with same CAS 130-26-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 305.50 g/mol
Formula C₉H₅ClINO
badge Registry Numbers
EC Number 204-984-4
MDL Number MFCD00006787
thermostat Physical Properties
Melting Point 175-183 °C
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

Used primarily in the synthesis of complex organic compounds, particularly in the development of pharmaceutical agents. It serves as a key intermediate in the production of antimicrobial and antiparasitic drugs, leveraging its halogenated structure to enhance biological activity. Additionally, it is employed in research settings to study quinoline derivatives for potential therapeutic applications, including treatments for infections and diseases caused by resistant pathogens. Its unique chemical structure also makes it valuable in materials science for creating specialized coatings or sensors.

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Test Parameter Specification
Purity (HPLC) 95-100
Purity (Nonaqueous Titration) 98-100
Infrared Spectrometry Conforms To Structure
Proton NMR Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 10g
10-20 days ฿1,590.00
inventory 50g
10-20 days ฿5,380.00
inventory 250g
10-20 days ฿24,560.00

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5-Chloro-8-hydroxy-7-iodoquinoline
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Used primarily in the synthesis of complex organic compounds, particularly in the development of pharmaceutical agents. It serves as a key intermediate in the production of antimicrobial and antiparasitic drugs, leveraging its halogenated structure to enhance biological activity. Additionally, it is employed in research settings to study quinoline derivatives for potential therapeutic applications, including treatments for infections and diseases caused by resistant pathogens. Its unique chemical structu

Used primarily in the synthesis of complex organic compounds, particularly in the development of pharmaceutical agents. It serves as a key intermediate in the production of antimicrobial and antiparasitic drugs, leveraging its halogenated structure to enhance biological activity. Additionally, it is employed in research settings to study quinoline derivatives for potential therapeutic applications, including treatments for infections and diseases caused by resistant pathogens. Its unique chemical structure also makes it valuable in materials science for creating specialized coatings or sensors.

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