3-Bromo-2-iodophenol
97%
Reagent
Code: #117005
CAS Number
855836-52-1
blur_circular Chemical Specifications
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Molecular Information
Weight
298.90 g/mol
Formula
C₆H₄BrIO
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Registry Numbers
MDL Number
MFCD08166320
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Physical Properties
Boiling Point
243.9°C at 760 mmHg
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Storage & Handling
Density
2.369g/cm3
Storage
2-8°C, protected from light, stored in an inert gas
description Product Description
3-Bromo-2-iodophenol is primarily utilized in organic synthesis as an intermediate for the preparation of more complex chemical compounds. Its halogenated structure makes it a valuable building block in the development of pharmaceuticals, particularly in the synthesis of active pharmaceutical ingredients (APIs) that require specific halogen substitutions for enhanced biological activity. Additionally, it is employed in the creation of agrochemicals, where its unique structure contributes to the efficacy of pesticides or herbicides. The compound is also used in material science for the synthesis of advanced organic materials, including liquid crystals or polymers, where its halogen atoms can influence the material's properties. In research, it serves as a reagent in cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are pivotal in constructing carbon-carbon bonds for various applications.
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3-Bromo-2-iodophenol
3-Bromo-2-iodophenol is primarily utilized in organic synthesis as an intermediate for the preparation of more complex chemical compounds. Its halogenated structure makes it a valuable building block in the development of pharmaceuticals, particularly in the synthesis of active pharmaceutical ingredients (APIs) that require specific halogen substitutions for enhanced biological activity. Additionally, it is employed in the creation of agrochemicals, where its unique structure contributes to the efficacy of pesticides or herbicides. The compound is also used in material science for the synthesis of advanced organic materials, including liquid crystals or polymers, where its halogen atoms can influence the material's properties. In research, it serves as a reagent in cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are pivotal in constructing carbon-carbon bonds for various applications.
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