4-(2,2,2-Trifluoroacetamido)benzoic acid

95%

Reagent Code: #46731
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CAS Number 404-26-2

science Other reagents with same CAS 404-26-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 233.1400 g/mol
Formula C₉H₆F₃NO₃
badge Registry Numbers
MDL Number MFCD00454055
thermostat Physical Properties
Boiling Point 370 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.539g/cm3
Storage room temperature

description Product Description

Used primarily in organic synthesis, this compound serves as a key intermediate in the production of pharmaceuticals and agrochemicals. Its trifluoroacetamido group enhances reactivity, making it valuable in peptide coupling reactions and the creation of complex organic molecules. Additionally, it is employed in the development of bioactive compounds, particularly in the modification of drug molecules to improve their pharmacokinetic properties. Its application extends to research settings where it aids in studying enzyme inhibition and receptor binding mechanisms.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance Off-White to Pink Solid
Purity (%) 94.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,872.00

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4-(2,2,2-Trifluoroacetamido)benzoic acid
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Used primarily in organic synthesis, this compound serves as a key intermediate in the production of pharmaceuticals and agrochemicals. Its trifluoroacetamido group enhances reactivity, making it valuable in peptide coupling reactions and the creation of complex organic molecules. Additionally, it is employed in the development of bioactive compounds, particularly in the modification of drug molecules to improve their pharmacokinetic properties. Its application extends to research settings where it aids

Used primarily in organic synthesis, this compound serves as a key intermediate in the production of pharmaceuticals and agrochemicals. Its trifluoroacetamido group enhances reactivity, making it valuable in peptide coupling reactions and the creation of complex organic molecules. Additionally, it is employed in the development of bioactive compounds, particularly in the modification of drug molecules to improve their pharmacokinetic properties. Its application extends to research settings where it aids in studying enzyme inhibition and receptor binding mechanisms.

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