2-Bromo-4-fluoro-1-(trifluoromethoxy)benzene

98%

Reagent Code: #79258
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CAS Number 866633-25-2

science Other reagents with same CAS 866633-25-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 259.00 g/mol
Formula C₇H₃BrF₄O
badge Registry Numbers
MDL Number MFCD11847187
thermostat Physical Properties
Boiling Point 174.2±35.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This chemical is primarily utilized in the field of organic synthesis, where it serves as a versatile building block for the development of more complex molecules. Its structure, featuring bromo and fluoro substituents, makes it particularly valuable in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, which are essential in pharmaceutical and agrochemical research. The trifluoromethoxy group enhances the lipophilicity of the resulting compounds, which can improve their bioavailability and metabolic stability. Additionally, it is employed in the synthesis of liquid crystals and advanced materials, where its unique electronic properties contribute to the desired performance characteristics. Its use in the creation of specialty chemicals and intermediates further highlights its importance in industrial and research applications.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,338.00
inventory 1g
10-20 days ฿9,882.00
inventory 100mg
10-20 days ฿2,907.00
inventory 5g
10-20 days ฿34,533.00

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2-Bromo-4-fluoro-1-(trifluoromethoxy)benzene
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This chemical is primarily utilized in the field of organic synthesis, where it serves as a versatile building block for the development of more complex molecules. Its structure, featuring bromo and fluoro substituents, makes it particularly valuable in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, which are essential in pharmaceutical and agrochemical research. The trifluoromethoxy group enhances the lipophilicity of the resulting compounds, which can improve their bioavailabil

This chemical is primarily utilized in the field of organic synthesis, where it serves as a versatile building block for the development of more complex molecules. Its structure, featuring bromo and fluoro substituents, makes it particularly valuable in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, which are essential in pharmaceutical and agrochemical research. The trifluoromethoxy group enhances the lipophilicity of the resulting compounds, which can improve their bioavailability and metabolic stability. Additionally, it is employed in the synthesis of liquid crystals and advanced materials, where its unique electronic properties contribute to the desired performance characteristics. Its use in the creation of specialty chemicals and intermediates further highlights its importance in industrial and research applications.

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