N-(2-Hydroxyethyl)-3-(4-nitrophenyl)propylamine

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Reagent Code: #217986
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CAS Number 130634-09-2

science Other reagents with same CAS 130634-09-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 224 g/mol
Formula C₁₁H₁₆N₂O₃
inventory_2 Storage & Handling
Storage 2-8℃, dry, closed

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and functional materials. Its structure contains both hydroxyl and amine groups, making it suitable for derivatization in drug development. Commonly employed in the preparation of dyes, sensors, and nitroaromatic-based compounds due to the electron-withdrawing nitro group enhancing reactivity in coupling reactions. Also explored in the design of bioactive molecules where the nitrophenyl moiety contributes to biological activity.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿840.00
inventory 1g
10-20 days ฿2,340.00
inventory 25g
10-20 days ฿33,200.00
inventory 5g
10-20 days ฿9,500.00

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N-(2-Hydroxyethyl)-3-(4-nitrophenyl)propylamine
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Used in organic synthesis as an intermediate for pharmaceuticals and functional materials. Its structure contains both hydroxyl and amine groups, making it suitable for derivatization in drug development. Commonly employed in the preparation of dyes, sensors, and nitroaromatic-based compounds due to the electron-withdrawing nitro group enhancing reactivity in coupling reactions. Also explored in the design of bioactive molecules where the nitrophenyl moiety contributes to biological activity.

Used in organic synthesis as an intermediate for pharmaceuticals and functional materials. Its structure contains both hydroxyl and amine groups, making it suitable for derivatization in drug development. Commonly employed in the preparation of dyes, sensors, and nitroaromatic-based compounds due to the electron-withdrawing nitro group enhancing reactivity in coupling reactions. Also explored in the design of bioactive molecules where the nitrophenyl moiety contributes to biological activity.

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