1-Bromo-2-iodo-4-methoxybenzene

≥95%

Reagent Code: #114755
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CAS Number 4897-68-1

science Other reagents with same CAS 4897-68-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 312.93 g/mol
Formula C₇H₆BrIO
badge Registry Numbers
MDL Number MFCD00070743
thermostat Physical Properties
Boiling Point 304.6°C at 760 mmHg
inventory_2 Storage & Handling
Density 2.063 g/cm3
Storage 2-8°C, dry and sealed away from light

description Product Description

Used primarily in organic synthesis, this compound serves as a versatile intermediate in the production of more complex molecules. Its bromo and iodo substituents make it highly reactive in cross-coupling reactions, such as Suzuki and Sonogashira couplings, enabling the formation of carbon-carbon bonds. The methoxy group can influence the electronic properties of the molecule, making it useful in the synthesis of pharmaceuticals, agrochemicals, and materials science applications. Additionally, its structure allows for selective functionalization, aiding in the development of specialized organic compounds.

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Test Parameter Specification
Appearance Colorless To Light Yellow Liquid
Purity (%) 94.5-100
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿6,680.00
inventory 250mg
10-20 days ฿820.00
inventory 1g
10-20 days ฿1,770.00

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1-Bromo-2-iodo-4-methoxybenzene
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Used primarily in organic synthesis, this compound serves as a versatile intermediate in the production of more complex molecules. Its bromo and iodo substituents make it highly reactive in cross-coupling reactions, such as Suzuki and Sonogashira couplings, enabling the formation of carbon-carbon bonds. The methoxy group can influence the electronic properties of the molecule, making it useful in the synthesis of pharmaceuticals, agrochemicals, and materials science applications. Additionally, its structure
Used primarily in organic synthesis, this compound serves as a versatile intermediate in the production of more complex molecules. Its bromo and iodo substituents make it highly reactive in cross-coupling reactions, such as Suzuki and Sonogashira couplings, enabling the formation of carbon-carbon bonds. The methoxy group can influence the electronic properties of the molecule, making it useful in the synthesis of pharmaceuticals, agrochemicals, and materials science applications. Additionally, its structure allows for selective functionalization, aiding in the development of specialized organic compounds.
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