2-Bromo-6-methylbenzonitrile

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Reagent Code: #80880
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CAS Number 77532-78-6

science Other reagents with same CAS 77532-78-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 196.04 g/mol
Formula C₈H₆BrN
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This compound is primarily used in organic synthesis as an intermediate for the production of various pharmaceuticals and agrochemicals. Its structure, featuring a bromine atom and a nitrile group, makes it a versatile building block for constructing more complex molecules. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to create biaryl structures commonly found in active pharmaceutical ingredients. Additionally, it serves as a precursor in the synthesis of herbicides and fungicides, where the nitrile group can be further modified to enhance biological activity. Its role in research and development is significant, particularly in the discovery of new compounds with potential therapeutic or agricultural applications.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿621.00
inventory 1g
10-20 days ฿1,512.00

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2-Bromo-6-methylbenzonitrile
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This compound is primarily used in organic synthesis as an intermediate for the production of various pharmaceuticals and agrochemicals. Its structure, featuring a bromine atom and a nitrile group, makes it a versatile building block for constructing more complex molecules. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to create biaryl structures commonly found in active pharmaceutical ingredients. Additionally, it serves as a precursor in the synthesis o

This compound is primarily used in organic synthesis as an intermediate for the production of various pharmaceuticals and agrochemicals. Its structure, featuring a bromine atom and a nitrile group, makes it a versatile building block for constructing more complex molecules. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to create biaryl structures commonly found in active pharmaceutical ingredients. Additionally, it serves as a precursor in the synthesis of herbicides and fungicides, where the nitrile group can be further modified to enhance biological activity. Its role in research and development is significant, particularly in the discovery of new compounds with potential therapeutic or agricultural applications.

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