Trifluoromethanesulfonic anhydride

98%

  • Product Code: 121858
  Alias:    Trifluoromethanesulfonic anhydride; trifluoromethanesulfonic anhydride, trifluoromethanesulfonic anhydride
  CAS:    358-23-6
Molecular Weight: 282.14 g./mol Molecular Formula: C₂F₆O₅S₂
EC Number: 206-616-8 MDL Number: MFCD00000408
Melting Point: -80°C Boiling Point: 81-83 °C(lit.)
Density: 1.677 g/mL at 25 °C(lit.) Storage Condition: 2~8°C
Product Description: Used primarily as a reagent in organic synthesis, it facilitates the introduction of the triflate group, which is a highly reactive leaving group. This property makes it valuable in forming carbon-carbon and carbon-heteroatom bonds, particularly in the synthesis of complex organic molecules. It is also employed in the preparation of sulfonate esters, which are crucial intermediates in pharmaceuticals and agrochemicals. Additionally, it serves as a catalyst or co-catalyst in various polymerization reactions, enhancing the efficiency of the process. Its strong electrophilic nature is exploited in Friedel-Crafts acylation reactions to produce aromatic ketones.
Product Specification:
Test Specification
Purity (%) 98-100
Refractive Index (N20/D) 1.321-1.323
Free Fluoride (As F) 300
CF3SO3H 0.5
Appearance Colorless To Brown Liquid
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
5.000 10-20 days ฿390.00
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10.000 10-20 days ฿760.00
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25.000 10-20 days ฿1,180.00
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100.000 10-20 days ฿3,290.00
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500.000 10-20 days ฿11,100.00
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Trifluoromethanesulfonic anhydride
Used primarily as a reagent in organic synthesis, it facilitates the introduction of the triflate group, which is a highly reactive leaving group. This property makes it valuable in forming carbon-carbon and carbon-heteroatom bonds, particularly in the synthesis of complex organic molecules. It is also employed in the preparation of sulfonate esters, which are crucial intermediates in pharmaceuticals and agrochemicals. Additionally, it serves as a catalyst or co-catalyst in various polymerization reactions, enhancing the efficiency of the process. Its strong electrophilic nature is exploited in Friedel-Crafts acylation reactions to produce aromatic ketones.
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