1,3-Dibromo-5-fluoro-2-iodobenzene

98%

Reagent Code: #114139
label
Alias 2,6-Dibromo-4-fluoroiodobenzene
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CAS Number 62720-29-0

science Other reagents with same CAS 62720-29-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 379.8 g/mol
Formula C₆H₂Br₂FI
badge Registry Numbers
MDL Number MFCD00042232
thermostat Physical Properties
Melting Point 134-137 °C
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily used as a versatile intermediate in organic synthesis, particularly in the development of complex molecules for pharmaceuticals and agrochemicals. Its unique halogen substitution pattern allows for selective functionalization, making it valuable in cross-coupling reactions such as Suzuki, Sonogashira, or Buchwald-Hartwig couplings. These reactions are crucial for constructing aromatic frameworks in drug discovery and material science. Additionally, it serves as a building block for synthesizing fluorinated and iodinated compounds, which are often explored for their biological activity or use in imaging agents. Its stability and reactivity make it a preferred choice in research and industrial applications.

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Test Parameter Specification
Melting Point 133-138
Purity (GC) 98-100%
Appearance White To Light Brown
Infrared Spectrum Conforms To Structure

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,000.00
inventory 1g
10-20 days ฿360.00
inventory 25g
10-20 days ฿3,860.00

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1,3-Dibromo-5-fluoro-2-iodobenzene
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This compound is primarily used as a versatile intermediate in organic synthesis, particularly in the development of complex molecules for pharmaceuticals and agrochemicals. Its unique halogen substitution pattern allows for selective functionalization, making it valuable in cross-coupling reactions such as Suzuki, Sonogashira, or Buchwald-Hartwig couplings. These reactions are crucial for constructing aromatic frameworks in drug discovery and material science. Additionally, it serves as a building block for synthesizing fluorinated and iodinated compounds, which are often explored for their biological activity or use in imaging agents. Its stability and reactivity make it a preferred choice in research and industrial applications.
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