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Merck

91737

Sigma-Aldrich

Anhídrido trifluorometanosulfónico

purum, ≥98.0% (T)

Sinónimos:

Anhídrido tríflico

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About This Item

Fórmula lineal:
(CF3SO2)2O
Número de CAS:
Peso molecular:
282.14
Beilstein/REAXYS Number:
1813600
EC Number:
MDL number:
UNSPSC Code:
12352101
PubChem Substance ID:
NACRES:
NA.22

vapor density

5.2 (vs air)

Quality Level

vapor pressure

8 mmHg ( 20 °C)

grade

purum

assay

≥98.0% (T)

form

liquid

refractive index

n20/D 1.321 (lit.)

bp

81-83 °C (lit.)

density

1.677 g/mL at 25 °C (lit.)

SMILES string

FC(F)(F)S(=O)(=O)OS(=O)(=O)C(F)(F)F

InChI

1S/C2F6O5S2/c3-1(4,5)14(9,10)13-15(11,12)2(6,7)8

InChI key

WJKHJLXJJJATHN-UHFFFAOYSA-N

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Application

Catalizador de la glucosilación para la síntesis de polisacáridos

Reactivo para la síntesis estereoselectiva de donantes de uronato de metil mannosazida

Activador de la glucosilación directa con hidroxiazúcares anómeros
Trifluoromethanesulfonic anhydride can be used in the preparation of azido sugars such as 6-azido fucose. It can also be used as a promoter for the Friedel-Crafts acylation of aromatic compounds with carboxylic acids in the absence of catalyst.
Tf2O in combination with:
  • Diphenyl sulfoxide, forms an efficient promoter system for the activation of thioglycosides for glycosylation reactions.
  • 2-chloropyridine, can be used for secondary amide activation.
  • Potassium iodide, can effectively mediate the deoxygenation of sulfoxides to form sulfides.
  • Hydrogen peroxide, for the selective oxidation of sulfanes to sulf­oxides in the presence of oxidatively sensitive functional groups.

Tf2O can react with:
  • Ketones in the presence of a base to form vinyl triflates.
  • Magnesium alkoxides to form corresponding symmetrical or unsymmetrical ethers.
  • Sodium azide for the in situ preparation of triflyl azide.

Other Notes

Electrophilic trifyl source. Reviews

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Ox. Liq. 2 - Skin Corr. 1B - STOT SE 3

target_organs

Respiratory system

Storage Class

5.1B - Oxidizing hazardous materials

wgk_germany

WGK 3

flash_point_f

not determinedboils before flash

flash_point_c

not determinedboils before flash

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter


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Los clientes también vieron

Synthesis, 85-85 (1982)
Synthesis of pyrimidines by direct condensation of amides and nitriles.
Movassaghi M & Hill MD.
Nature Protocols, 2(8), 2018-2018 (2007)
H2O2/Tf2O System: An efficient oxidizing reagent for selective oxidation of sulfanes.
Khodaei MM, et al.
Synthesis, 2008(11), 1682-1684 (2008)
Ether synthesis using trifluoromethanesulfonic anhydride or triflates under mild reaction conditions.
Nishiyama T, et al.
Canadian Journal of Chemistry, 77(2), 258-262 (1999)
Mild and efficient deoxygenation of sulfoxides to sulfides with triflic anhydride/potassium iodide reagent system.
Bahrami K, et al.
Synthesis, 2008(16), 2543-2546 (2008)

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