2-(2-Bromo-5-methoxyphenyl)acetonitrile

97%

Reagent Code: #115622
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CAS Number 27387-23-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 226.07 g/mol
Formula C₉H₈BrNO
badge Registry Numbers
MDL Number MFCD09927439
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

This chemical is primarily utilized in organic synthesis as a key intermediate for the production of various pharmaceuticals and agrochemicals. Its structure, featuring a bromo and methoxy substituent on the phenyl ring, makes it a valuable building block for constructing complex molecules. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce specific functional groups into target compounds. Additionally, it serves as a precursor in the synthesis of biologically active compounds, including potential drug candidates targeting neurological or inflammatory disorders. Its nitrile group also allows for further chemical transformations, such as hydrolysis or reduction, to yield carboxylic acids or amines, expanding its utility in diverse chemical processes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days €22.26
inventory 250mg
10-20 days €42.16
inventory 1g
10-20 days €107.53
inventory 5g
10-20 days €325.20
2-(2-Bromo-5-methoxyphenyl)acetonitrile
This chemical is primarily utilized in organic synthesis as a key intermediate for the production of various pharmaceuticals and agrochemicals. Its structure, featuring a bromo and methoxy substituent on the phenyl ring, makes it a valuable building block for constructing complex molecules. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce specific functional groups into target compounds. Additionally, it serves as a precursor in the synthesis of biologically active compounds, including potential drug candidates targeting neurological or inflammatory disorders. Its nitrile group also allows for further chemical transformations, such as hydrolysis or reduction, to yield carboxylic acids or amines, expanding its utility in diverse chemical processes.
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