4-Fluoro-N-methyl-2-nitrobenzamide

98%

Reagent Code: #215532
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CAS Number 1018983-85-1

science Other reagents with same CAS 1018983-85-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 198.15 g/mol
Formula C₈H₇FN₂O₃
badge Registry Numbers
MDL Number MFCD26799386
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of selective enzyme inhibitors and bioactive molecules. Its structure supports derivatization for use in medicinal chemistry research, especially in studies targeting neurological and inflammatory pathways. Also employed in agrochemical research for designing novel active ingredients due to its electron-withdrawing groups and aromatic stability. The compound's nitro and fluoro functionalities make it suitable for cross-coupling reactions and functional group transformations in organic synthesis.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿9,580.00
inventory 1g
10-20 days ฿25,840.00

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4-Fluoro-N-methyl-2-nitrobenzamide
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of selective enzyme inhibitors and bioactive molecules. Its structure supports derivatization for use in medicinal chemistry research, especially in studies targeting neurological and inflammatory pathways. Also employed in agrochemical research for designing novel active ingredients due to its electron-withdrawing groups and aromatic stability. The compound's nitro and fluoro functionalities make it sui

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of selective enzyme inhibitors and bioactive molecules. Its structure supports derivatization for use in medicinal chemistry research, especially in studies targeting neurological and inflammatory pathways. Also employed in agrochemical research for designing novel active ingredients due to its electron-withdrawing groups and aromatic stability. The compound's nitro and fluoro functionalities make it suitable for cross-coupling reactions and functional group transformations in organic synthesis.

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