6-Bromo-2-fluoro-3-methylbenzonitrile

95%

Reagent Code: #49858
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CAS Number 1501163-33-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 214.0344 g/mol
Formula C₈H₅BrFN
badge Registry Numbers
MDL Number MFCD26680100
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily used in the pharmaceutical and agrochemical industries as a key intermediate in the synthesis of more complex molecules. Its structure, featuring both bromo and fluoro substituents, makes it a versatile building block for creating compounds with specific biological activities. In pharmaceuticals, it is often utilized in the development of active pharmaceutical ingredients (APIs) targeting various diseases, including central nervous system disorders and cancer. In agrochemicals, it serves as a precursor in the production of herbicides and pesticides, where its unique halogenated structure contributes to the efficacy of the final product. Additionally, its nitrile group allows for further functionalization, enabling the creation of diverse chemical derivatives for research and industrial applications.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days €195.07
inventory 250mg
10-20 days €316.60
inventory 5g
10-20 days €1,354.96
inventory 10g
10-20 days €2,356.15
inventory 1g
10-20 days €693.03
6-Bromo-2-fluoro-3-methylbenzonitrile
This compound is primarily used in the pharmaceutical and agrochemical industries as a key intermediate in the synthesis of more complex molecules. Its structure, featuring both bromo and fluoro substituents, makes it a versatile building block for creating compounds with specific biological activities. In pharmaceuticals, it is often utilized in the development of active pharmaceutical ingredients (APIs) targeting various diseases, including central nervous system disorders and cancer. In agrochemicals, it serves as a precursor in the production of herbicides and pesticides, where its unique halogenated structure contributes to the efficacy of the final product. Additionally, its nitrile group allows for further functionalization, enabling the creation of diverse chemical derivatives for research and industrial applications.
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