2,2,2-Trifluoro-N-(prop-2-yn-1-yl)acetamide

98%

Reagent Code: #71789
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CAS Number 14719-21-2

science Other reagents with same CAS 14719-21-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 151.09 g/mol
Formula C₅H₄F₃NO
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily utilized in organic synthesis as a versatile building block for the creation of more complex molecules. Its trifluoroacetamide group is particularly valuable in peptide chemistry, where it serves as a protective group for amines, ensuring selective reactions during synthesis. Additionally, the propynyl moiety enables participation in click chemistry reactions, such as the copper-catalyzed azide-alkyne cycloaddition (CuAAC), which is widely used in bioconjugation and drug discovery. Its applications extend to the development of pharmaceuticals, agrochemicals, and materials science, where its unique structure contributes to the design of compounds with enhanced stability and reactivity.

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Test Parameter Specification
Appearance Colorless to light yellow liquid
Purity 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿11,580.00
inventory 50mg
10-20 days ฿390.00
inventory 250mg
10-20 days ฿920.00
inventory 1g
10-20 days ฿2,610.00

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2,2,2-Trifluoro-N-(prop-2-yn-1-yl)acetamide
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This chemical is primarily utilized in organic synthesis as a versatile building block for the creation of more complex molecules. Its trifluoroacetamide group is particularly valuable in peptide chemistry, where it serves as a protective group for amines, ensuring selective reactions during synthesis. Additionally, the propynyl moiety enables participation in click chemistry reactions, such as the copper-catalyzed azide-alkyne cycloaddition (CuAAC), which is widely used in bioconjugation and drug discov

This chemical is primarily utilized in organic synthesis as a versatile building block for the creation of more complex molecules. Its trifluoroacetamide group is particularly valuable in peptide chemistry, where it serves as a protective group for amines, ensuring selective reactions during synthesis. Additionally, the propynyl moiety enables participation in click chemistry reactions, such as the copper-catalyzed azide-alkyne cycloaddition (CuAAC), which is widely used in bioconjugation and drug discovery. Its applications extend to the development of pharmaceuticals, agrochemicals, and materials science, where its unique structure contributes to the design of compounds with enhanced stability and reactivity.

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