1-Bromo-3-fluoro-5-(trifluoromethoxy)benzene

95%

Reagent Code: #40020
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CAS Number 1129541-09-8

science Other reagents with same CAS 1129541-09-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 258.9957 g/mol
Formula C₇H₃BrF₄O
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MDL Number MFCD22551456
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description Product Description

This chemical is primarily utilized in the field of organic synthesis, particularly as a building block for the development of complex molecules. Its unique structure, featuring bromo, fluoro, and trifluoromethoxy substituents, makes it valuable in the creation of pharmaceuticals and agrochemicals. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce aromatic frameworks with specific functional groups. Additionally, its fluorine-containing groups enhance the metabolic stability and bioavailability of the resulting compounds, making it a key intermediate in drug discovery and material science.

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inventory 100mg
10-20 days ฿4,824.00

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1-Bromo-3-fluoro-5-(trifluoromethoxy)benzene
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This chemical is primarily utilized in the field of organic synthesis, particularly as a building block for the development of complex molecules. Its unique structure, featuring bromo, fluoro, and trifluoromethoxy substituents, makes it valuable in the creation of pharmaceuticals and agrochemicals. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce aromatic frameworks with specific functional groups. Additionally, its fluorine-containing groups en

This chemical is primarily utilized in the field of organic synthesis, particularly as a building block for the development of complex molecules. Its unique structure, featuring bromo, fluoro, and trifluoromethoxy substituents, makes it valuable in the creation of pharmaceuticals and agrochemicals. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce aromatic frameworks with specific functional groups. Additionally, its fluorine-containing groups enhance the metabolic stability and bioavailability of the resulting compounds, making it a key intermediate in drug discovery and material science.

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