1-Ethynyl-2-(trifluoromethyl)benzene

97%

Reagent Code: #240648
label
Alias 1-Alkynyl-2-(trifluoromethyl)benzene, trifluoromethylphenylacetylene, 2-ethynyl-α,α,α-trifluorotoluene, 2-ethynyltrifluorotoluene
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CAS Number 704-41-6

science Other reagents with same CAS 704-41-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 170.13 g/mol
Formula C₉H₅F₃
badge Registry Numbers
MDL Number MFCD00467313
thermostat Physical Properties
Boiling Point 45°C 8mm Hg (Lit.)
inventory_2 Storage & Handling
Density 1.2220g/ml
Storage Room temperature

description Product Description

Used primarily as a building block in organic synthesis, especially in pharmaceuticals and agrochemicals. Its alkyne functionality allows participation in coupling reactions such as Sonogashira and click chemistry, enabling the construction of complex molecules. The electron-withdrawing trifluoromethyl group enhances stability and influences reactivity, making it valuable in the development of bioactive compounds. It is also employed in materials science for designing fluorinated organic semiconductors and specialty polymers with improved thermal and oxidative stability.

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿168.00
inventory 5g
10-20 days ฿2,910.00
inventory 25g
10-20 days ฿14,250.00
inventory 1g
10-20 days ฿600.00

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1-Ethynyl-2-(trifluoromethyl)benzene
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Used primarily as a building block in organic synthesis, especially in pharmaceuticals and agrochemicals. Its alkyne functionality allows participation in coupling reactions such as Sonogashira and click chemistry, enabling the construction of complex molecules. The electron-withdrawing trifluoromethyl group enhances stability and influences reactivity, making it valuable in the development of bioactive compounds. It is also employed in materials science for designing fluorinated organic semiconductors a

Used primarily as a building block in organic synthesis, especially in pharmaceuticals and agrochemicals. Its alkyne functionality allows participation in coupling reactions such as Sonogashira and click chemistry, enabling the construction of complex molecules. The electron-withdrawing trifluoromethyl group enhances stability and influences reactivity, making it valuable in the development of bioactive compounds. It is also employed in materials science for designing fluorinated organic semiconductors and specialty polymers with improved thermal and oxidative stability.

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