Methyl 2-(bromomethyl)-6-iodobenzoate

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Reagent Code: #83283
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CAS Number 861840-51-9

science Other reagents with same CAS 861840-51-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 354.97 g/mol
Formula C₉H₈BrIO₂
badge Registry Numbers
MDL Number MFCD20529140
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in an inert gas

description Product Description

This compound is primarily utilized in organic synthesis as a versatile intermediate. Its structure, featuring both bromomethyl and iodo substituents, makes it a valuable building block for constructing complex molecules, particularly in pharmaceutical research. The bromomethyl group is highly reactive and can participate in nucleophilic substitution reactions, enabling the introduction of various functional groups. The iodo substituent is useful in cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential for creating carbon-carbon bonds in drug development. Additionally, the ester group provides a handle for further derivatization, making it a flexible precursor in the synthesis of biologically active compounds. Its applications are particularly relevant in the preparation of heterocycles and other aromatic systems used in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,913.00
inventory 250mg
10-20 days ฿8,829.00
inventory 1g
10-20 days ฿21,987.00

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Methyl 2-(bromomethyl)-6-iodobenzoate
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This compound is primarily utilized in organic synthesis as a versatile intermediate. Its structure, featuring both bromomethyl and iodo substituents, makes it a valuable building block for constructing complex molecules, particularly in pharmaceutical research. The bromomethyl group is highly reactive and can participate in nucleophilic substitution reactions, enabling the introduction of various functional groups. The iodo substituent is useful in cross-coupling reactions, such as Suzuki or Sonogashira

This compound is primarily utilized in organic synthesis as a versatile intermediate. Its structure, featuring both bromomethyl and iodo substituents, makes it a valuable building block for constructing complex molecules, particularly in pharmaceutical research. The bromomethyl group is highly reactive and can participate in nucleophilic substitution reactions, enabling the introduction of various functional groups. The iodo substituent is useful in cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential for creating carbon-carbon bonds in drug development. Additionally, the ester group provides a handle for further derivatization, making it a flexible precursor in the synthesis of biologically active compounds. Its applications are particularly relevant in the preparation of heterocycles and other aromatic systems used in medicinal chemistry.

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