3,4-Difluoro-5-methylbenzonitrile

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Reagent Code: #178433
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CAS Number 1803833-51-3

science Other reagents with same CAS 1803833-51-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 153.13 g/mol
Formula C₈H₅F₂N
badge Registry Numbers
MDL Number MFCD22490588
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) for central nervous system (CNS) drugs and kinase inhibitors. Its fluorinated aromatic structure enhances metabolic stability and bioavailability in drug candidates. Also employed in agrochemicals for the production of herbicides and fungicides due to its electron-withdrawing nitrile group and fluorine substitution, which improve target selectivity and environmental persistence. Commonly utilized in research and development for structure-activity relationship (SAR) studies in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,820.00
inventory 250mg
10-20 days ฿6,310.00
inventory 1g
10-20 days ฿20,370.00

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3,4-Difluoro-5-methylbenzonitrile
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) for central nervous system (CNS) drugs and kinase inhibitors. Its fluorinated aromatic structure enhances metabolic stability and bioavailability in drug candidates. Also employed in agrochemicals for the production of herbicides and fungicides due to its electron-withdrawing nitrile group and fluorine substitution, which improve target selectivity and environmental

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) for central nervous system (CNS) drugs and kinase inhibitors. Its fluorinated aromatic structure enhances metabolic stability and bioavailability in drug candidates. Also employed in agrochemicals for the production of herbicides and fungicides due to its electron-withdrawing nitrile group and fluorine substitution, which improve target selectivity and environmental persistence. Commonly utilized in research and development for structure-activity relationship (SAR) studies in medicinal chemistry.

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