1-Bromo-4-chloro-2-fluorobenzene

98%

Reagent Code: #114789
label
Alias 2-bromo-5-chlorofluorobenzene 4-chloro-2-fluorobromobenzene
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CAS Number 1996-29-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 209.44 g/mol
Formula C₆H₃BrClF
badge Registry Numbers
MDL Number MFCD00079708
thermostat Physical Properties
Boiling Point 91-92 °C20 mm Hg(lit.)
inventory_2 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

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿360.00
inventory 100g
10-20 days ฿3,740.00
inventory 25g
10-20 days ฿1,070.00
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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