2-Bromo-5-fluoro-3-nitrobenzoic acid

95%

Reagent Code: #64246
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CAS Number 1055331-73-1

science Other reagents with same CAS 1055331-73-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 264.01 g/mol
Formula C₇H₃BrFNO₄
badge Registry Numbers
MDL Number MFCD12173018
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

This compound is primarily utilized in organic synthesis as a versatile intermediate for the development of more complex molecules. Its structure, featuring bromo, fluoro, and nitro functional groups, makes it a valuable building block in pharmaceutical research, particularly in the synthesis of active pharmaceutical ingredients (APIs). It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to create novel compounds with potential therapeutic applications. Additionally, its nitro group can be reduced to an amine, further expanding its utility in medicinal chemistry for designing drug candidates. The presence of fluorine enhances the metabolic stability and bioavailability of the resulting molecules, making it a key component in the development of advanced pharmaceuticals.

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Test Parameter Specification
Appearance White to Light Yellow Solid
Purity (%) 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,465.00
inventory 100mg
10-20 days ฿846.00
inventory 250mg
10-20 days ฿1,395.00

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2-Bromo-5-fluoro-3-nitrobenzoic acid
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This compound is primarily utilized in organic synthesis as a versatile intermediate for the development of more complex molecules. Its structure, featuring bromo, fluoro, and nitro functional groups, makes it a valuable building block in pharmaceutical research, particularly in the synthesis of active pharmaceutical ingredients (APIs). It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to create novel compounds with potential therapeutic applications. Additionally, its nitro group can be reduced to an amine, further expanding its utility in medicinal chemistry for designing drug candidates. The presence of fluorine enhances the metabolic stability and bioavailability of the resulting molecules, making it a key component in the development of advanced pharmaceuticals.
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