4-Fluoroiodobenzene

99%, including 0.01% copper stabilizer

Reagent Code: #118941
label
Alias 4-fluoroiodobenzene; p-fluoroiodobenzene, 1-fluoro-4-iodobenzene
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CAS Number 352-34-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 222 g/mol
Formula C₆H₄FI
badge Registry Numbers
EC Number 206-522-7
MDL Number MFCD00001052
thermostat Physical Properties
Melting Point −20 °C(lit.)
Boiling Point 182-184 °C(lit.)
inventory_2 Storage & Handling
Density 1.925 g/mL at 25 °C(lit.)
Storage Room temperature, away from light, dry

description Product Description

4-Fluoroiodobenzene is widely used as a versatile intermediate in organic synthesis, particularly in the preparation of complex molecules. It serves as a key building block in the development of pharmaceuticals, where it is employed in cross-coupling reactions such as Suzuki, Sonogashira, and Heck reactions to introduce aromatic fluorine and iodine substituents. These reactions are crucial for creating biologically active compounds, including potential drug candidates. Additionally, it is utilized in material science for synthesizing advanced organic materials, such as liquid crystals and polymers, due to its ability to modify electronic and structural properties. Its role in agrochemical research is also notable, as it aids in the development of novel pesticides and herbicides.

format_list_bulleted Product Specification

Test Parameter Specification
Purity (GC) 99-100
Refractive Index (N20/D) 1.582-1.584
Specific Gravity (20/20) 1.91-1.921
Appearance Colorless to light yellow clear liquid
Infrared Spectrum Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 500g
10-20 days ฿9,860.00
inventory 100g
10-20 days ฿2,450.00
inventory 25g
10-20 days ฿890.00
inventory 5g
10-20 days ฿290.00
4-Fluoroiodobenzene
4-Fluoroiodobenzene is widely used as a versatile intermediate in organic synthesis, particularly in the preparation of complex molecules. It serves as a key building block in the development of pharmaceuticals, where it is employed in cross-coupling reactions such as Suzuki, Sonogashira, and Heck reactions to introduce aromatic fluorine and iodine substituents. These reactions are crucial for creating biologically active compounds, including potential drug candidates. Additionally, it is utilized in material science for synthesizing advanced organic materials, such as liquid crystals and polymers, due to its ability to modify electronic and structural properties. Its role in agrochemical research is also notable, as it aids in the development of novel pesticides and herbicides.
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