(2-Bromo-5-iodophenyl)methanol

98%

Reagent Code: #74202
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CAS Number 946525-30-0

science Other reagents with same CAS 946525-30-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 312.93 g/mol
Formula C₇H₆BrIO
badge Registry Numbers
MDL Number MFCD11044842
thermostat Physical Properties
Melting Point 112-116°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in organic synthesis as a versatile intermediate for constructing complex molecules. Its unique structure, featuring both bromo and iodo substituents, makes it a valuable building block in cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential in pharmaceutical and materials chemistry. Additionally, the presence of the methanol group allows for further functionalization, enabling the creation of diverse derivatives for use in drug discovery and development. Its role in synthesizing biologically active compounds, particularly in medicinal chemistry, highlights its significance in research and industrial applications.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿810.00
inventory 5g
10-20 days ฿2,394.00

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(2-Bromo-5-iodophenyl)methanol
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This compound is primarily utilized in organic synthesis as a versatile intermediate for constructing complex molecules. Its unique structure, featuring both bromo and iodo substituents, makes it a valuable building block in cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential in pharmaceutical and materials chemistry. Additionally, the presence of the methanol group allows for further functionalization, enabling the creation of diverse derivatives for use in drug discov

This compound is primarily utilized in organic synthesis as a versatile intermediate for constructing complex molecules. Its unique structure, featuring both bromo and iodo substituents, makes it a valuable building block in cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential in pharmaceutical and materials chemistry. Additionally, the presence of the methanol group allows for further functionalization, enabling the creation of diverse derivatives for use in drug discovery and development. Its role in synthesizing biologically active compounds, particularly in medicinal chemistry, highlights its significance in research and industrial applications.

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