4-(4-Nitrophenoxy)Benzaldehyde

≥98%

Reagent Code: #220221
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CAS Number 50961-54-1

science Other reagents with same CAS 50961-54-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 243.21 g/mol
Formula C₁₃H₉NO₄
badge Registry Numbers
MDL Number MFCD06496623
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of liquid crystal materials, particularly in the production of advanced display technologies. Its structure supports the formation of thermally stable and optically anisotropic compounds essential for LCDs. Also employed in the preparation of pharmaceuticals and agrochemicals due to its reactive aldehyde and nitro groups, which allow further functionalization. Additionally, it serves as a building block in organic synthesis for creating Schiff bases and other nitrogen-containing heterocycles with potential biological activity.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,720.00
inventory 1g
10-20 days ฿4,820.00
inventory 5g
10-20 days ฿18,800.00
4-(4-Nitrophenoxy)Benzaldehyde
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Used as an intermediate in the synthesis of liquid crystal materials, particularly in the production of advanced display technologies. Its structure supports the formation of thermally stable and optically anisotropic compounds essential for LCDs. Also employed in the preparation of pharmaceuticals and agrochemicals due to its reactive aldehyde and nitro groups, which allow further functionalization. Additionally, it serves as a building block in organic synthesis for creating Schiff bases and other nitr

Used as an intermediate in the synthesis of liquid crystal materials, particularly in the production of advanced display technologies. Its structure supports the formation of thermally stable and optically anisotropic compounds essential for LCDs. Also employed in the preparation of pharmaceuticals and agrochemicals due to its reactive aldehyde and nitro groups, which allow further functionalization. Additionally, it serves as a building block in organic synthesis for creating Schiff bases and other nitrogen-containing heterocycles with potential biological activity.

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