4-Iodobenzyl bromide

97%

Reagent Code: #119560
label
Alias p-Iodobenzyl bromide; 4-iodobenzyl bromide
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CAS Number 16004-15-2

science Other reagents with same CAS 16004-15-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 296.93 g/mol
Formula C₇H₆BrI
badge Registry Numbers
MDL Number MFCD00209656
thermostat Physical Properties
Melting Point 78-82 °C(lit.)
Boiling Point 140°C 15mm
inventory_2 Storage & Handling
Storage 2~8°C, away from light

description Product Description

Used primarily as a reagent in organic synthesis, 4-Iodobenzyl bromide is valuable for introducing the 4-iodobenzyl group into molecules. It is commonly employed in the preparation of pharmaceuticals, particularly in the synthesis of complex organic compounds. The compound is also utilized in the development of materials for organic electronics, where it acts as a building block for creating functionalized aromatic systems. Additionally, it finds application in cross-coupling reactions, such as Suzuki and Heck reactions, which are essential for constructing carbon-carbon bonds in advanced chemical research.

format_list_bulleted Product Specification

Test Parameter Specification
Melting Point 78-82°C
Purity (GC) 96.5-100%
Purity (Titration By AgNO3 After O2 Combustion) 96.5-103.5%
Purity (Titration By AgNO3 After O2 Combustion) 96.5-103.5%
Appearance White To Beige Powder Or Crystals
Infrared Spectrum Conforms To Structure
Proton NMR Spectrum Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100g
10-20 days ฿20,160.00
inventory 1g
10-20 days ฿380.00
inventory 25g
10-20 days ฿5,600.00
inventory 5g
10-20 days ฿1,210.00

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4-Iodobenzyl bromide
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Used primarily as a reagent in organic synthesis, 4-Iodobenzyl bromide is valuable for introducing the 4-iodobenzyl group into molecules. It is commonly employed in the preparation of pharmaceuticals, particularly in the synthesis of complex organic compounds. The compound is also utilized in the development of materials for organic electronics, where it acts as a building block for creating functionalized aromatic systems. Additionally, it finds application in cross-coupling reactions, such as Suzuki and Heck reactions, which are essential for constructing carbon-carbon bonds in advanced chemical research.
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