1-Ethyl-4-[2-(4-methylphenyl)-1-ethynyl]benzene

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Reagent Code: #182230
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CAS Number 22692-80-4

science Other reagents with same CAS 22692-80-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 220.31 g/mol
Formula C₁₇H₁₆
badge Registry Numbers
MDL Number MFCD04038793
thermostat Physical Properties
Melting Point 71-74°C
Boiling Point 135-136 °C (1 mmHg)
inventory_2 Storage & Handling
Density 1.02
Storage Room temperature, seal, dry

description Product Description

Used primarily in organic synthesis and materials science, this compound serves as a building block for conjugated systems in the development of organic semiconductors and optoelectronic devices. Its rigid, planar structure with extended π-conjugation makes it suitable for applications in organic light-emitting diodes (OLEDs) and field-effect transistors (OFETs). It is also employed in the synthesis of advanced polymers and liquid crystals, where molecular rigidity and electronic properties are critical. Additionally, its alkyne functionality allows for use in click chemistry and palladium-catalyzed coupling reactions, facilitating the construction of complex molecular architectures in pharmaceutical and agrochemical research.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿690.00
inventory 25g
10-20 days ฿3,220.00
inventory 500g
10-20 days ฿35,740.00
inventory 100g
10-20 days ฿11,060.00

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1-Ethyl-4-[2-(4-methylphenyl)-1-ethynyl]benzene
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Used primarily in organic synthesis and materials science, this compound serves as a building block for conjugated systems in the development of organic semiconductors and optoelectronic devices. Its rigid, planar structure with extended π-conjugation makes it suitable for applications in organic light-emitting diodes (OLEDs) and field-effect transistors (OFETs). It is also employed in the synthesis of advanced polymers and liquid crystals, where molecular rigidity and electronic properties are critical. Additionally, its alkyne functionality allows for use in click chemistry and palladium-catalyzed coupling reactions, facilitating the construction of complex molecular architectures in pharmaceutical and agrochemical research.
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