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MERCURY(II) TRIFLUOROMETHANESULFONATE

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MERCURY(II) TRIFLUOROMETHANESULFONATE Basic information

Product Name:
MERCURY(II) TRIFLUOROMETHANESULFONATE
Synonyms:
  • MERCURY(II) TRIFLUOROMETHANESULFONATE (MERCURY TRIFLATE)
  • Mercury(Ⅱ) trifluoroMethanesulfonate
  • Hg(OTf)2
  • Methanesulfonic acid,1,1,1-trifluoro-, mercury(2+) salt (2:1)
  • Mercury trifluoromethanesulfonate
  • MERCURY(II) TRIFLUOROMETHANESULFONATE
  • MERCURY(II) TRIFLUOROMETHANESULPHONATE
  • MERCURY TRIFLATE
CAS:
49540-00-3
MF:
CHF3HgO3S
MW:
350.66
Product Categories:
  • metal triflate compounds
  • triflate
  • Catalysis and Inorganic Chemistry
  • Chemical Synthesis
  • Mercury
Mol File:
49540-00-3.mol
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MERCURY(II) TRIFLUOROMETHANESULFONATE Chemical Properties

Melting point:
>350 °C (lit.)
solubility 
It is soluble in H2O and CH3CN, fairly soluble in CH3NO2 and CH2Cl2, insoluble in hexane, ether, and toluene.
form 
Powder
color 
White
Sensitive 
Moisture Sensitive
Exposure limits
NIOSH: IDLH 10 mg/m3; TWA 0.05 mg/m3; Ceiling 0.1 mg/m3
Stability:
hygroscopic
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Safety Information

Hazard Codes 
T+,N,T,C
Risk Statements 
26/27/28-33-50/53
Safety Statements 
13-28-36-45-60-61
RIDADR 
UN 2025 6.1/PG 2
WGK Germany 
3
Hazard Note 
Corrosive/Toxic
HazardClass 
6.1
PackingGroup 
II
HS Code 
28521000

MSDS

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MERCURY(II) TRIFLUOROMETHANESULFONATE Usage And Synthesis

Uses

Hg(OTf)2 exhibits remarkable catalytic activity for the hydroxylative cyclization of 1,6-enynes. Mercuric triflate is a very versatile reagent and has been used for several organic catalytic transformations including C-C bond forming cyclizations, alkyne hydrations, heterocycle synthesis and very recently in C-N bond forming reactions. Commonly used as the metal source for Lewis acid catalyzed asymmetric reactions.

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