N-(5-Fluoro-2-nitrophenyl)acetamide

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Reagent Code: #215624
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CAS Number 345-14-2

science Other reagents with same CAS 345-14-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 198.15 g/mol
Formula C₈H₇FN₂O₃
badge Registry Numbers
MDL Number MFCD09836765
thermostat Physical Properties
Boiling Point 378.4±32.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.429±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of fluorinated dyes and pigments, particularly in the production of azo dyes where the nitro group can be reduced and diazotized for coupling reactions. Its fluorine substituent enhances electron-withdrawing properties, improving dye fastness and color stability. Also employed in the preparation of certain pharmaceuticals, where it serves as a building block for active ingredients targeting anti-inflammatory or antimicrobial applications. Additionally, it finds use in agrochemical synthesis, contributing to the development of herbicides and pesticides due to its stability and reactivity profile.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,520.00
inventory 250mg
10-20 days ฿11,010.00
inventory 1g
10-20 days ฿29,720.00

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N-(5-Fluoro-2-nitrophenyl)acetamide
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Used as an intermediate in the synthesis of fluorinated dyes and pigments, particularly in the production of azo dyes where the nitro group can be reduced and diazotized for coupling reactions. Its fluorine substituent enhances electron-withdrawing properties, improving dye fastness and color stability. Also employed in the preparation of certain pharmaceuticals, where it serves as a building block for active ingredients targeting anti-inflammatory or antimicrobial applications. Additionally, it finds us

Used as an intermediate in the synthesis of fluorinated dyes and pigments, particularly in the production of azo dyes where the nitro group can be reduced and diazotized for coupling reactions. Its fluorine substituent enhances electron-withdrawing properties, improving dye fastness and color stability. Also employed in the preparation of certain pharmaceuticals, where it serves as a building block for active ingredients targeting anti-inflammatory or antimicrobial applications. Additionally, it finds use in agrochemical synthesis, contributing to the development of herbicides and pesticides due to its stability and reactivity profile.

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