6-Amino-3-bromo-2-fluorobenzoic acid

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Reagent Code: #120509
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CAS Number 1036756-03-2

science Other reagents with same CAS 1036756-03-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 234.02 g/mol
Formula C₇H₅BrFNO₂
badge Registry Numbers
MDL Number MFCD20482512
thermostat Physical Properties
Boiling Point 335.3±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.877±0.06 g/cm3(Predicted)
Storage Room temperature, dark, inert gas

description Product Description

This chemical is primarily utilized in organic synthesis, particularly as a building block for the development of more complex molecules. Its structure, featuring amino, bromo, and fluoro substituents, makes it a valuable intermediate in the preparation of pharmaceuticals, agrochemicals, and specialty chemicals. The bromo and fluoro groups are often leveraged in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, to create biologically active compounds. Additionally, the amino group allows for further functionalization, enabling the synthesis of diverse derivatives. Its applications are particularly significant in medicinal chemistry, where it contributes to the creation of drug candidates targeting various diseases.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿23,148.00
inventory 1g
10-20 days ฿1,836.00
inventory 5g
10-20 days ฿6,201.00

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6-Amino-3-bromo-2-fluorobenzoic acid
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This chemical is primarily utilized in organic synthesis, particularly as a building block for the development of more complex molecules. Its structure, featuring amino, bromo, and fluoro substituents, makes it a valuable intermediate in the preparation of pharmaceuticals, agrochemicals, and specialty chemicals. The bromo and fluoro groups are often leveraged in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, to create biologically active compounds. Additionally, the amino group allows for further functionalization, enabling the synthesis of diverse derivatives. Its applications are particularly significant in medicinal chemistry, where it contributes to the creation of drug candidates targeting various diseases.
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