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49540-00-3

49540-00-3 Structure

49540-00-3 Structure
IdentificationBack Directory
[Name]

MERCURY(II) TRIFLUOROMETHANESULFONATE
[CAS]

49540-00-3
[Synonyms]

Hg(OTf)2
MERCURY TRIFLATE
mercuric triflate
mercury(ii) triflate
Mercury(II) Triflate (2:1)
Mercury trifluoromethanesulfonate
Mercury(Ⅱ) trifluoroMethanesulfonate
MERCURY(II) TRIFLUOROMETHANESULFONATE
MERCURY(II) TRIFLUOROMETHANESULPHONATE
Mercury(II)trifluoromethanesulfonate,98%
MERCURY(II) TRIFLUOROMETHANESULFONATE 98%
MercurytrifluoromethanesulfonateMercurytriflatepowder
Mercury(II) trifluoromethanesulfonate, 99.9% metals basis
MERCURY(II) TRIFLUOROMETHANESULFONATE (MERCURY TRIFLATE)
Methanesulfonic acid,1,1,1-trifluoro-, mercury(2+) salt (2:1)
MERCURY (II) TRIFLUOROMETHANESULFONATE 98% (MERCURY TRIFLATE)
[Molecular Formula]

C2F6HgO6S2
[MDL Number]

MFCD00144746
[MOL File]

49540-00-3.mol
[Molecular Weight]

498.73
Chemical PropertiesBack Directory
[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
[InChI]

1S/2CHF3O3S.Hg/c2*2-1(3,4)8(5,6)7;/h2*(H,5,6,7);/q;;+2/p-2
[InChIKey]

BPVYMDMPLCOQPJ-UHFFFAOYSA-L
[SMILES]

[Hg++].[O-]S(=O)(=O)C(F)(F)F.[O-]S(=O)(=O)C(F)(F)F
Safety DataBack Directory
[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
[Storage Class]

6.1A - Combustible acute toxic Cat. 1 and 2
very toxic hazardous materials
[Hazard Classifications]

Acute Tox. 1 Dermal
Acute Tox. 2 Inhalation
Acute Tox. 2 Oral
Aquatic Acute 1
Aquatic Chronic 1
STOT RE 2
Hazard InformationBack Directory
[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.
[reaction suitability]

core: mercury
reagent type: catalyst
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