2,6-Difluoro-3-methylbenzyl bromide

95%

  • Product Code: 62266
  CAS:    261763-44-4
Molecular Weight: 221.04 g./mol Molecular Formula: C₈H₇BrF₂
EC Number: MDL Number: MFCD01631336
Melting Point: Boiling Point:
Density: Storage Condition: 2-8°C, dry, sealed
Product Description: This compound is primarily used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. Its structure, featuring both fluorine and bromine substituents, makes it a valuable building block for creating more complex molecules. It is often employed in cross-coupling reactions, such as Suzuki or Sonogashira couplings, to introduce fluorinated aromatic groups into target compounds. This is especially useful in drug development, where fluorine atoms can enhance the bioavailability and metabolic stability of pharmaceutical agents. Additionally, it serves as a precursor in the synthesis of herbicides and pesticides, where the fluorine atoms contribute to the efficacy of the final product. Its reactivity with various nucleophiles also makes it a versatile reagent in the preparation of specialty chemicals.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.250 10-20 days $49.72
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1.000 10-20 days $89.95
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2,6-Difluoro-3-methylbenzyl bromide
This compound is primarily used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. Its structure, featuring both fluorine and bromine substituents, makes it a valuable building block for creating more complex molecules. It is often employed in cross-coupling reactions, such as Suzuki or Sonogashira couplings, to introduce fluorinated aromatic groups into target compounds. This is especially useful in drug development, where fluorine atoms can enhance the bioavailability and metabolic stability of pharmaceutical agents. Additionally, it serves as a precursor in the synthesis of herbicides and pesticides, where the fluorine atoms contribute to the efficacy of the final product. Its reactivity with various nucleophiles also makes it a versatile reagent in the preparation of specialty chemicals.
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