N-benzyl-4-nitrobenzenamine

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Reagent Code: #218451
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CAS Number 14309-92-3

science Other reagents with same CAS 14309-92-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 228.25 g/mol
Formula C₁₃H₁₂N₂O₂
badge Registry Numbers
MDL Number MFCD00126504
thermostat Physical Properties
Boiling Point 392ºC at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its structure allows for further functionalization through reduction of the nitro group or modification of the amine, making it valuable in constructing complex nitrogen-containing molecules. Commonly employed in the development of dyes and pigments due to its aromatic and electron-withdrawing properties. Also finds use in research settings for synthesizing compounds with biological activity, including potential antimicrobial or antitumor agents.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,310.00
inventory 1g
10-20 days ฿3,520.00
inventory 5g
10-20 days ฿14,550.00

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N-benzyl-4-nitrobenzenamine
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its structure allows for further functionalization through reduction of the nitro group or modification of the amine, making it valuable in constructing complex nitrogen-containing molecules. Commonly employed in the development of dyes and pigments due to its aromatic and electron-withdrawing properties. Also finds use in research settings for synthesizing compounds with biological activity,
Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its structure allows for further functionalization through reduction of the nitro group or modification of the amine, making it valuable in constructing complex nitrogen-containing molecules. Commonly employed in the development of dyes and pigments due to its aromatic and electron-withdrawing properties. Also finds use in research settings for synthesizing compounds with biological activity, including potential antimicrobial or antitumor agents.
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