1-Bromo-4-chloro-2-fluorobenzene

98%

  • Product Code: 114789
  Alias:    2-bromo-5-chlorofluorobenzene 4-chloro-2-fluorobromobenzene
  CAS:    1996-29-8
Molecular Weight: 209.44 g./mol Molecular Formula: C₆H₃BrClF
EC Number: MDL Number: MFCD00079708
Melting Point: Boiling Point: 91-92 °C20 mm Hg(lit.)
Density: 1.678 g/mL at 25 °C(lit.) Storage Condition: room temperature
Product Description: 1-Bromo-4-chloro-2-fluorobenzene is primarily used as an intermediate in organic synthesis, particularly in the pharmaceutical and agrochemical industries. It serves as a building block for the development of more complex molecules, including active pharmaceutical ingredients (APIs) and crop protection agents. Its unique halogen substitution pattern makes it valuable for introducing specific functional groups into target compounds. Additionally, it is employed in research and development for creating novel chemical entities, especially in the field of medicinal chemistry, where it aids in the design of drugs with enhanced biological activity. Its role in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, is also notable, enabling the construction of diverse aromatic systems.
Product Specification:
Test Specification
Purity (%) 98-100
Refractive Index (20 Degree Celsius) 1.554-1.558
Appearance Colorless To Light Yellow Liquid
Infrared Spectrum Conforms To Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
5.000 10-20 days ฿360.00
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25.000 10-20 days ฿1,070.00
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100.000 10-20 days ฿3,740.00
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1-Bromo-4-chloro-2-fluorobenzene
1-Bromo-4-chloro-2-fluorobenzene is primarily used as an intermediate in organic synthesis, particularly in the pharmaceutical and agrochemical industries. It serves as a building block for the development of more complex molecules, including active pharmaceutical ingredients (APIs) and crop protection agents. Its unique halogen substitution pattern makes it valuable for introducing specific functional groups into target compounds. Additionally, it is employed in research and development for creating novel chemical entities, especially in the field of medicinal chemistry, where it aids in the design of drugs with enhanced biological activity. Its role in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, is also notable, enabling the construction of diverse aromatic systems.
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