4-Ethynyl-α,α,α-trifluorotoluene

97%

Reagent Code: #66346
label
Alias [4-(Trifluoromethyl)phenyl]acetylene; 4-Ethynylbenzotrifluoride; 4-Ethynyl-α,α,α-benzotrifluoride
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CAS Number 705-31-7

science Other reagents with same CAS 705-31-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 170.13 g/mol
Formula C₉H₅F₃
badge Registry Numbers
MDL Number MFCD01861903
inventory_2 Storage & Handling
Storage room temperature, sealed

description Product Description

Used primarily in organic synthesis, this compound serves as a key building block for creating more complex molecules. Its ethynyl group allows for versatile reactions, such as click chemistry, enabling the formation of triazoles. The trifluoromethyl group enhances the stability and lipophilicity of resulting compounds, making it valuable in pharmaceutical research for drug development. It is also employed in materials science to design advanced polymers and coatings with unique properties. Additionally, its structural features make it useful in agrochemical research for developing novel pesticides and herbicides.

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Test Parameter Specification
Purity 96.5-100%
Refractive Index n20D 1.463-1.467
Appearance Colorless to pale yellow

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿4,800.00
inventory 1g
10-20 days ฿1,560.00
inventory 200mg
10-20 days ฿520.00
inventory 25g
10-20 days ฿15,600.00

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4-Ethynyl-α,α,α-trifluorotoluene
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Used primarily in organic synthesis, this compound serves as a key building block for creating more complex molecules. Its ethynyl group allows for versatile reactions, such as click chemistry, enabling the formation of triazoles. The trifluoromethyl group enhances the stability and lipophilicity of resulting compounds, making it valuable in pharmaceutical research for drug development. It is also employed in materials science to design advanced polymers and coatings with unique properties. Additionally,

Used primarily in organic synthesis, this compound serves as a key building block for creating more complex molecules. Its ethynyl group allows for versatile reactions, such as click chemistry, enabling the formation of triazoles. The trifluoromethyl group enhances the stability and lipophilicity of resulting compounds, making it valuable in pharmaceutical research for drug development. It is also employed in materials science to design advanced polymers and coatings with unique properties. Additionally, its structural features make it useful in agrochemical research for developing novel pesticides and herbicides.

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