4-Bromo-8-(trifluoromethoxy)quinoline

≥95%

Reagent Code: #86154
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CAS Number 1189105-60-9

science Other reagents with same CAS 1189105-60-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 292.05 g/mol
Formula C₁₀H₅BrF₃NO
badge Registry Numbers
MDL Number MFCD12674964
thermostat Physical Properties
Boiling Point 293.8°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of more complex quinoline derivatives. These derivatives are often explored for their potential pharmacological properties, particularly in the development of new therapeutic agents. Its unique structure, featuring both bromine and trifluoromethoxy groups, makes it a valuable building block in medicinal chemistry for creating compounds with potential anti-inflammatory, antimicrobial, or anticancer activities. Additionally, it is used in research to study the effects of halogen and trifluoromethoxy substitutions on the biological activity of quinoline-based molecules.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿6,930.00
inventory 100mg
10-20 days ฿360.00
inventory 250mg
10-20 days ฿657.00
inventory 1g
10-20 days ฿1,971.00

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4-Bromo-8-(trifluoromethoxy)quinoline
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This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of more complex quinoline derivatives. These derivatives are often explored for their potential pharmacological properties, particularly in the development of new therapeutic agents. Its unique structure, featuring both bromine and trifluoromethoxy groups, makes it a valuable building block in medicinal chemistry for creating compounds with potential anti-inflammatory, antimicrobial, or anticancer activities. Additionally, it is used in research to study the effects of halogen and trifluoromethoxy substitutions on the biological activity of quinoline-based molecules.
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