Methyl 2-bromo-4-iodobenzoate

97%

Reagent Code: #116709
label
Alias 2-Bromo-4-iodobenzoic acid methyl ester; Benzoic acid, 2-bromo-4-iodo-, methyl ester
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CAS Number 1261588-35-5

science Other reagents with same CAS 1261588-35-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 340.94 g/mol
Formula C₈H₆BrIO₂
badge Registry Numbers
MDL Number MFCD11870175
inventory_2 Storage & Handling
Storage Room temperature, dry out of light

description Product Description

Methyl 2-bromo-4-iodobenzoate is primarily used as a versatile intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its structure, featuring both bromo and iodo substituents, makes it a valuable building block for cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential for constructing complex molecules. This compound is also employed in the synthesis of biologically active compounds, including potential drug candidates, due to its ability to introduce functional groups at specific positions on the aromatic ring. Additionally, it serves as a precursor in the preparation of advanced materials and specialty chemicals, where precise molecular design is critical.

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Test Parameter Specification
Appearance Light Yellow To Light Brown Solid
Purity (%) 96.5-100%
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿972.00
inventory 5g
10-20 days ฿3,465.00

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Methyl 2-bromo-4-iodobenzoate
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Methyl 2-bromo-4-iodobenzoate is primarily used as a versatile intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its structure, featuring both bromo and iodo substituents, makes it a valuable building block for cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential for constructing complex molecules. This compound is also employed in the synthesis of biologically active compounds, including potential drug candidates, due to its ability to introduce functional groups at specific positions on the aromatic ring. Additionally, it serves as a precursor in the preparation of advanced materials and specialty chemicals, where precise molecular design is critical.
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