1-Bromo-4-fluoro-2-nitro-5-(trifluoromethyl)benzene

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Reagent Code: #40040
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CAS Number 889459-13-6

science Other reagents with same CAS 889459-13-6

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Weight 287.9900 g/mol
Formula C₇H₂BrF₄NO₂
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MDL Number MFCD12827971
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description Product Description

Used primarily as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. Its structure, featuring multiple functional groups including bromine, fluorine, nitro, and trifluoromethyl, allows for versatile reactivity, making it valuable in the development of complex molecules. It is often employed in cross-coupling reactions to create biologically active compounds. Additionally, its electron-withdrawing groups enhance its utility in nucleophilic aromatic substitution reactions, facilitating the introduction of other functional groups. This compound is also explored in material science for the synthesis of specialty chemicals and advanced materials.

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inventory 250mg
10-20 days ฿2,520.00

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1-Bromo-4-fluoro-2-nitro-5-(trifluoromethyl)benzene
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Used primarily as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. Its structure, featuring multiple functional groups including bromine, fluorine, nitro, and trifluoromethyl, allows for versatile reactivity, making it valuable in the development of complex molecules. It is often employed in cross-coupling reactions to create biologically active compounds. Additionally, its electron-withdrawing groups enhance its utility in nucleophilic aromatic s

Used primarily as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. Its structure, featuring multiple functional groups including bromine, fluorine, nitro, and trifluoromethyl, allows for versatile reactivity, making it valuable in the development of complex molecules. It is often employed in cross-coupling reactions to create biologically active compounds. Additionally, its electron-withdrawing groups enhance its utility in nucleophilic aromatic substitution reactions, facilitating the introduction of other functional groups. This compound is also explored in material science for the synthesis of specialty chemicals and advanced materials.

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