3,4,5-Trifluorocinnamic acid

97%

Reagent Code: #240011
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CAS Number 152152-19-7

science Other reagents with same CAS 152152-19-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 202.13 g/mol
Formula CF₃C₆H₂CH=CHCO₂H
badge Registry Numbers
MDL Number MFCD00083529
thermostat Physical Properties
Melting Point 195-199 °C(lit.)
Boiling Point 273.8±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.468±0.06 g/cm3(Predicted)
Storage 2-8°C, Inert Gas

description Product Description

Used in the synthesis of fluorinated organic compounds, particularly in pharmaceuticals and agrochemicals where fluorine substitution enhances metabolic stability and bioavailability. Acts as a building block in medicinal chemistry for developing biologically active molecules, including potential antitumor and antimicrobial agents. Also employed in materials science for designing liquid crystals and functional polymers with improved thermal and electronic properties due to the electron-withdrawing effect of fluorine atoms. Its conjugated structure supports applications in photoresponsive materials and UV-absorbing compounds.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,570.00
inventory 25g
10-20 days ฿6,800.00
3,4,5-Trifluorocinnamic acid
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Used in the synthesis of fluorinated organic compounds, particularly in pharmaceuticals and agrochemicals where fluorine substitution enhances metabolic stability and bioavailability. Acts as a building block in medicinal chemistry for developing biologically active molecules, including potential antitumor and antimicrobial agents. Also employed in materials science for designing liquid crystals and functional polymers with improved thermal and electronic properties due to the electron-withdrawing effect

Used in the synthesis of fluorinated organic compounds, particularly in pharmaceuticals and agrochemicals where fluorine substitution enhances metabolic stability and bioavailability. Acts as a building block in medicinal chemistry for developing biologically active molecules, including potential antitumor and antimicrobial agents. Also employed in materials science for designing liquid crystals and functional polymers with improved thermal and electronic properties due to the electron-withdrawing effect of fluorine atoms. Its conjugated structure supports applications in photoresponsive materials and UV-absorbing compounds.

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