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

98%

  • Product Code: 71789
  CAS:    14719-21-2
Molecular Weight: 151.09 g./mol Molecular Formula: C₅H₄F₃NO
EC Number: MDL Number:
Melting Point: Boiling Point:
Density: Storage Condition: 2-8°C
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.
Product Specification:
Test Specification
APPEARANCE Colorless to light yellow Liquid
PURITY 97.5-100
Infrared spectrum Conforms to Structure
NMR Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.050 10-20 days ฿390.00
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-
0.250 10-20 days ฿920.00
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1.000 10-20 days ฿2,610.00
+
-
5.000 10-20 days ฿11,580.00
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-
2,2,2-Trifluoro-N-(prop-2-yn-1-yl)acetamide
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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