3-(Trifluoromethyl)phenylacetylene

98%

Reagent Code: #242363
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CAS Number 705-28-2

science Other reagents with same CAS 705-28-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 170.13 g/mol
Formula C₉H₅F₃
badge Registry Numbers
MDL Number MFCD00467355
thermostat Physical Properties
Boiling Point 146 °C-lit.
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in organic synthesis, particularly in cross-coupling reactions such as Sonogashira coupling, to construct complex molecules for pharmaceuticals and agrochemicals. Its electron-withdrawing trifluoromethyl group enhances reactivity and stability in conjugated systems, making it valuable in materials science for developing organic semiconductors and liquid crystals. Also employed in the preparation of fluorinated analogs in medicinal chemistry to improve metabolic stability and bioavailability of drug candidates.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿162.00
1g
10-20 days ฿880.00
5g
10-20 days ฿4,080.00
25g
10-20 days ฿16,300.00
3-(Trifluoromethyl)phenylacetylene
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Used in organic synthesis, particularly in cross-coupling reactions such as Sonogashira coupling, to construct complex molecules for pharmaceuticals and agrochemicals. Its electron-withdrawing trifluoromethyl group enhances reactivity and stability in conjugated systems, making it valuable in materials science for developing organic semiconductors and liquid crystals. Also employed in the preparation of fluorinated analogs in medicinal chemistry to improve metabolic stability and bioavailability of drug can
Used in organic synthesis, particularly in cross-coupling reactions such as Sonogashira coupling, to construct complex molecules for pharmaceuticals and agrochemicals. Its electron-withdrawing trifluoromethyl group enhances reactivity and stability in conjugated systems, making it valuable in materials science for developing organic semiconductors and liquid crystals. Also employed in the preparation of fluorinated analogs in medicinal chemistry to improve metabolic stability and bioavailability of drug candidates.
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