2-Bromo-3-fluoro-6-nitrobenzoic acid

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Reagent Code: #64244
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CAS Number 881415-27-6

science Other reagents with same CAS 881415-27-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 264.01 g/mol
Formula C₇H₃BrFNO₄
badge Registry Numbers
MDL Number MFCD27931341
thermostat Physical Properties
Boiling Point 364.3±42.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

This chemical is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of complex molecules, particularly in the synthesis of active pharmaceutical ingredients (APIs). Its unique structure, featuring bromo, fluoro, and nitro substituents, makes it valuable for constructing compounds with specific electronic and steric properties. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to create biologically active compounds. Additionally, it is used in the study of structure-activity relationships (SAR) to optimize drug efficacy and selectivity. Its applications extend to agrochemical research, where it aids in the development of novel pesticides and herbicides.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿9,000.00
inventory 250mg
10-20 days ฿3,600.00
inventory 100mg
10-20 days ฿2,232.00

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2-Bromo-3-fluoro-6-nitrobenzoic acid
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This chemical is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of complex molecules, particularly in the synthesis of active pharmaceutical ingredients (APIs). Its unique structure, featuring bromo, fluoro, and nitro substituents, makes it valuable for constructing compounds with specific electronic and steric properties. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to create biolo

This chemical is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of complex molecules, particularly in the synthesis of active pharmaceutical ingredients (APIs). Its unique structure, featuring bromo, fluoro, and nitro substituents, makes it valuable for constructing compounds with specific electronic and steric properties. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to create biologically active compounds. Additionally, it is used in the study of structure-activity relationships (SAR) to optimize drug efficacy and selectivity. Its applications extend to agrochemical research, where it aids in the development of novel pesticides and herbicides.

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