Methyl 4-bromo-2-fluoro-5-nitrobenzoate

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Reagent Code: #47377
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CAS Number 1153285-35-8

science Other reagents with same CAS 1153285-35-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 278.03 g/mol
Formula C₈H₅BrFNO₄
badge Registry Numbers
MDL Number MFCD12173001
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

This compound is primarily used in organic synthesis as a versatile intermediate for the preparation of more complex molecules. Its structure, featuring bromo, fluoro, and nitro substituents, makes it highly reactive in various chemical transformations, such as nucleophilic aromatic substitution and coupling reactions. It is often employed in the development of pharmaceuticals and agrochemicals, where the nitro group can be reduced to an amine for further functionalization. Additionally, the ester group allows for easy hydrolysis or transesterification, enabling the incorporation of the aromatic core into larger structures. Its applications also extend to materials science, where it can be used to synthesize specialized polymers or dyes with specific properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,736.00
inventory 250mg
10-20 days ฿4,644.00
inventory 1g
10-20 days ฿12,528.00

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Methyl 4-bromo-2-fluoro-5-nitrobenzoate
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This compound is primarily used in organic synthesis as a versatile intermediate for the preparation of more complex molecules. Its structure, featuring bromo, fluoro, and nitro substituents, makes it highly reactive in various chemical transformations, such as nucleophilic aromatic substitution and coupling reactions. It is often employed in the development of pharmaceuticals and agrochemicals, where the nitro group can be reduced to an amine for further functionalization. Additionally, the ester group

This compound is primarily used in organic synthesis as a versatile intermediate for the preparation of more complex molecules. Its structure, featuring bromo, fluoro, and nitro substituents, makes it highly reactive in various chemical transformations, such as nucleophilic aromatic substitution and coupling reactions. It is often employed in the development of pharmaceuticals and agrochemicals, where the nitro group can be reduced to an amine for further functionalization. Additionally, the ester group allows for easy hydrolysis or transesterification, enabling the incorporation of the aromatic core into larger structures. Its applications also extend to materials science, where it can be used to synthesize specialized polymers or dyes with specific properties.

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