2-Bromo-3-iodophenol

97%

Reagent Code: #116660
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CAS Number 863870-88-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 298.9 g/mol
Formula C₆H₄BrIO
badge Registry Numbers
MDL Number MFCD08166322
thermostat Physical Properties
Melting Point 69-71 °C
Boiling Point 290.1±25.0 °C(Predicted)
inventory_2 Storage & Handling
Density 2.369±0.06 g/cm3(Predicted)
Storage 2-8℃, shading

description Product Description

2-Bromo-3-iodophenol is primarily used in organic synthesis as a versatile intermediate. It is often employed in the preparation of complex molecules, particularly in the pharmaceutical industry, where it serves as a building block for the synthesis of active pharmaceutical ingredients (APIs). Its unique halogenated structure makes it valuable in cross-coupling reactions, such as Suzuki and Sonogashira reactions, which are crucial for creating carbon-carbon bonds in drug development. Additionally, it finds applications in material science, where it is used to synthesize specialized polymers and organic compounds with specific electronic or optical properties. Its role in research and development is significant, particularly in the study of halogenated aromatic compounds and their reactivity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days £56.77
inventory 250mg
10-20 days £97.71
2-Bromo-3-iodophenol
2-Bromo-3-iodophenol is primarily used in organic synthesis as a versatile intermediate. It is often employed in the preparation of complex molecules, particularly in the pharmaceutical industry, where it serves as a building block for the synthesis of active pharmaceutical ingredients (APIs). Its unique halogenated structure makes it valuable in cross-coupling reactions, such as Suzuki and Sonogashira reactions, which are crucial for creating carbon-carbon bonds in drug development. Additionally, it finds applications in material science, where it is used to synthesize specialized polymers and organic compounds with specific electronic or optical properties. Its role in research and development is significant, particularly in the study of halogenated aromatic compounds and their reactivity.
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