2-([1,1'-Biphenyl]-3-yl)-4-chloro-6-phenyl-1,3,5-triazine

≥98%(GC)

Reagent Code: #149392
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CAS Number 1689576-03-1

science Other reagents with same CAS 1689576-03-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 343.81 g/mol
Formula C₂₁H₁₄ClN₃
badge Registry Numbers
MDL Number MFCD30531632
thermostat Physical Properties
Melting Point 141 °C
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

This compound is primarily used as a synthetic intermediate for constructing complex organic structures, especially in organic electronics research such as organic light-emitting diodes (OLEDs) and organic solar cells. Its stable triazine core provides excellent electron conductivity and specific light absorption in targeted wavelengths, making it ideal for electron energy transfer systems. The chlorine substituent enables facile nucleophilic aromatic substitutions for further functionalization. Additionally, it is developed as a catalyst in high-precision pharmaceutical synthesis processes.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿310.00
inventory 5g
10-20 days ฿1,250.00
inventory 25g
10-20 days ฿5,180.00

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2-([1,1'-Biphenyl]-3-yl)-4-chloro-6-phenyl-1,3,5-triazine
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This compound is primarily used as a synthetic intermediate for constructing complex organic structures, especially in organic electronics research such as organic light-emitting diodes (OLEDs) and organic solar cells. Its stable triazine core provides excellent electron conductivity and specific light absorption in targeted wavelengths, making it ideal for electron energy transfer systems. The chlorine substituent enables facile nucleophilic aromatic substitutions for further functionalization. Addition

This compound is primarily used as a synthetic intermediate for constructing complex organic structures, especially in organic electronics research such as organic light-emitting diodes (OLEDs) and organic solar cells. Its stable triazine core provides excellent electron conductivity and specific light absorption in targeted wavelengths, making it ideal for electron energy transfer systems. The chlorine substituent enables facile nucleophilic aromatic substitutions for further functionalization. Additionally, it is developed as a catalyst in high-precision pharmaceutical synthesis processes.

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