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MERCURY(II) TRIFLUOROMETHANESULFONATE

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Products Intro: Product Name:MERCURY(II) TRIFLUOROMETHANESULFONATE
CAS:49540-00-3
Purity:0.98 Package:1KG;10KG;50KG
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Products Intro: Product Name:MERCURY(II) TRIFLUOROMETHANESULFONATE
CAS:49540-00-3
Purity:0.99 Package:5KG;1KG
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Products Intro: Product Name:MERCURY(II) TRIFLUOROMETHANESULFONATE
CAS:49540-00-3
Purity:99% Package:25kg;5KG;1KG
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Products Intro: Product Name:mercury(ii) trifluoromethanesulphonate
CAS:49540-00-3
Purity:99% Package:1kg
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Products Intro: Product Name:MERCURY(II) TRIFLUOROMETHANESULFONATE
CAS:49540-00-3
Purity:99% Package:1g;1USD

MERCURY(II) TRIFLUOROMETHANESULFONATE manufacturers
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
EINECS:
Product Categories:metal triflate compounds;triflate;Catalysis and Inorganic Chemistry;Chemical Synthesis;Mercury
Mol File:49540-00-3.mol
MERCURY(II) TRIFLUOROMETHANESULFONATE Structure
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 limitsNIOSH: IDLH 10 mg/m3; TWA 0.05 mg/m3; Ceiling 0.1 mg/m3
Stability:hygroscopic
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 Information
ProviderLanguage
SigmaAldrich English
ALFA English
MERCURY(II) TRIFLUOROMETHANESULFONATE Usage And Synthesis
UsesHg(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.
MERCURY(II) TRIFLUOROMETHANESULFONATE Preparation Products And Raw materials
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