1-Bromo-2,4,6-trifluorobenzene

98%

  • Product Code: 114735
  Alias:    2-Bromo-1,3,5-trifluorobenzene 2,4,6-trifluorobromobenzene
  CAS:    2367-76-2
Molecular Weight: 210.98 g./mol Molecular Formula: BrC₆H₂F₃
EC Number: 219-125-9 MDL Number: MFCD00000334
Melting Point: 3.5 °C(lit.) Boiling Point: 140.5 °C(lit.)
Density: 1.79 g/mL at 25 °C(lit.) Storage Condition: room temperature, flammable area
Product Description: 1-Bromo-2,4,6-trifluorobenzene is primarily used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. Its unique structure, featuring both bromine and fluorine substituents, makes it a valuable building block for creating complex molecules. In the pharmaceutical industry, it is often employed in the development of active pharmaceutical ingredients (APIs) due to its ability to introduce fluorine atoms, which can enhance the biological activity and metabolic stability of drugs. Additionally, it finds use in the synthesis of specialty chemicals and materials, where its halogenated aromatic ring can be further functionalized to create compounds with specific properties. Its role in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, is also notable, enabling the construction of diverse aromatic systems.
Product Specification:
Test Specification
Purity (GC) 98-100
Refractive Index N20/D 1.483-1.485
Specific Gravity (20/20) 1.796-1.803
Appearance Colorless To Yellow Liquid
Infrared Spectrum Conforms To Structure
Note This Product Is Low Melting Point Solid, May Change State In Different Environments (Solid, Liquid Or Semi-Solid)
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿580.00
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5.000 10-20 days ฿1,980.00
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1-Bromo-2,4,6-trifluorobenzene
1-Bromo-2,4,6-trifluorobenzene is primarily used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. Its unique structure, featuring both bromine and fluorine substituents, makes it a valuable building block for creating complex molecules. In the pharmaceutical industry, it is often employed in the development of active pharmaceutical ingredients (APIs) due to its ability to introduce fluorine atoms, which can enhance the biological activity and metabolic stability of drugs. Additionally, it finds use in the synthesis of specialty chemicals and materials, where its halogenated aromatic ring can be further functionalized to create compounds with specific properties. Its role in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, is also notable, enabling the construction of diverse aromatic systems.
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