1-Bromo-4-chloro-2-fluorobenzene
98%
Reagent
Code: #114789
Alias
2-bromo-5-chlorofluorobenzene 4-chloro-2-fluorobromobenzene
CAS Number
1996-29-8
blur_circular Chemical Specifications
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Molecular Information
Weight
209.44 g/mol
Formula
C₆H₃BrClF
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Registry Numbers
MDL Number
MFCD00079708
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Physical Properties
Boiling Point
91-92 °C20 mm Hg(lit.)
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Storage & Handling
Density
1.678 g/mL at 25 °C(lit.)
Storage
room temperature
description 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.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Purity (%) | 98-100% |
Refractive Index (20°C) | 1.554-1.558 |
Appearance | Colorless to light yellow liquid |
Infrared Spectrum | Conforms To Structure |
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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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