4-methoxy-N-(4-nitrophenyl)benzenamine

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Reagent Code: #214661
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CAS Number 730-11-0

science Other reagents with same CAS 730-11-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 244.25 g/mol
Formula C₁₃H₁₂N₂O₃
badge Registry Numbers
MDL Number MFCD00550442
inventory_2 Storage & Handling
Storage 2-8℃, dry, sealed

description Product Description

Used as an intermediate in the synthesis of dyes and pigments, particularly in the production of azo dyes due to its aromatic amine functionality. Its electron-donating methoxy group and electron-withdrawing nitro group make it suitable for use in charge-transfer complexes and nonlinear optical materials. Also employed in the development of certain pharmaceuticals and agrochemicals where substituted anilines are required. Its structure allows for coupling reactions in the preparation of functional organic compounds for research and industrial applications.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,650.00
inventory 250mg
10-20 days ฿8,010.00
inventory 1g
10-20 days ฿23,850.00

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4-methoxy-N-(4-nitrophenyl)benzenamine
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Used as an intermediate in the synthesis of dyes and pigments, particularly in the production of azo dyes due to its aromatic amine functionality. Its electron-donating methoxy group and electron-withdrawing nitro group make it suitable for use in charge-transfer complexes and nonlinear optical materials. Also employed in the development of certain pharmaceuticals and agrochemicals where substituted anilines are required. Its structure allows for coupling reactions in the preparation of functional organi

Used as an intermediate in the synthesis of dyes and pigments, particularly in the production of azo dyes due to its aromatic amine functionality. Its electron-donating methoxy group and electron-withdrawing nitro group make it suitable for use in charge-transfer complexes and nonlinear optical materials. Also employed in the development of certain pharmaceuticals and agrochemicals where substituted anilines are required. Its structure allows for coupling reactions in the preparation of functional organic compounds for research and industrial applications.

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