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Bismuth(III) trifluoromethanesulfonate

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Bismuth(III) trifluoromethanesulfonate Basic information

Product Name:
Bismuth(III) trifluoromethanesulfonate
Synonyms:
  • BISMUTH(III)TRIFLATE
  • BISMUTH(III) TRIFLUOROMETHANESULFONATE
  • BISMUTH(III)TRIFLUOROMETHANESULPHONATE
  • BISMUTH TRIFLATE
  • BISMUTH TRIFLUOROMETHANESULFONATE HYDRATE
  • BISMUTH TRIFLUOROMETHANESULFONATE, ANHY&
  • Trifluoromethanesulfonicacidbismuthsalt
  • Bismuth(III)trifluoromethanesulfonate,min.98%(Bismuthtriflate)
CAS:
88189-03-1
MF:
3CF3O3S.Bi
MW:
656.18
Product Categories:
  • metal triflate compound
  • triflate
  • Bismuth
  • Catalysis and Inorganic Chemistry
  • Chemical Synthesis
Mol File:
88189-03-1.mol
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Bismuth(III) trifluoromethanesulfonate Chemical Properties

Melting point:
300 °C
storage temp. 
Inert atmosphere,Room Temperature
solubility 
Soluble in organics acetonitrile, dioxane, dimethyl formamide and dimethyl sulfoxide.
form 
Liquid
color 
Clear colorless
Sensitive 
Hygroscopic
Hydrolytic Sensitivity
5: forms reversible hydrate
Stability:
hygroscopic
InChIKey
HIYUMYXSGIKHHE-UHFFFAOYSA-M
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-24/25
WGK Germany 
3
Hazard Note 
Irritant
TSCA 
No
HazardClass 
8
HS Code 
29049090

MSDS

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Bismuth(III) trifluoromethanesulfonate Usage And Synthesis

Uses

Bismuth(III) trifluoromethanesulfonate is powerful Lewis acid useful in a number of catalytic reactions. 

Chemical Properties

White powder

Uses

Bismuth(III) trifluoromethanesulfonate acts as a catalyst in Friedel-Crafts acylation and cycloisomerization of allene-enol ethers. It behaves as a direct substitution catalyst and involved in the substitution of allylic, propargylic, and benzylic alcohols with sulfonamides, carboxamides and carbamates. Further, it is also used in Mukaiyama aldol reactions.

Uses

Catalyzes direct substitution of allylic, propargylic, and benzylic alcohols with sulfonamides, carbamates, and carboxamides.

Uses

Catalyst for organic syntheses.

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