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HAFNIUM TRIFLUOROMETHANESULFONATE

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HAFNIUM TRIFLUOROMETHANESULFONATE Basic information

Product Name:
HAFNIUM TRIFLUOROMETHANESULFONATE
Synonyms:
  • TRIFLUOROMETHANESULFONIC ACID HAFNIUM(4) SALT
  • TRIFLUOROMETHANESULFONIC ACID HAFNIUM(IV) SALT
  • HAFNIUM TRIFLATE
  • HAFNIUM TRIFLUOROMETHANESULFONATE
  • HAFNIUM(IV) TRIFLATE
  • HAFNIUM(IV) TRIFLUOROMETHANESULFONATE
  • HAFNIUM (IV) TRIFLUOROMETHANESULPHONATE
  • HAFNIUM TRIFLUOROMETHANESULFONATE HYDRAT E
CAS:
161337-67-3
MF:
CHF3HfO3S
MW:
328.56
Mol File:
161337-67-3.mol
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HAFNIUM TRIFLUOROMETHANESULFONATE Chemical Properties

Melting point:
>350 °C(lit.)
Flash point:
None
solubility 
Soluble in methyl cyanide, dicholomethane, dichloroethane, nitromethane, dioxane, terahydrofuran and toluene.
form 
powder to crystal
color 
White to Light yellow
Sensitive 
Hygroscopic
Exposure limits
ACGIH: TWA 0.5 mg/m3
NIOSH: IDLH 50 mg/m3; TWA 0.5 mg/m3
CAS DataBase Reference
161337-67-3(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
RIDADR 
UN 1759 8/PG III
WGK Germany 
3
Hazard Note 
Irritant
HazardClass 
8
PackingGroup 
III
HS Code 
29049090

MSDS

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HAFNIUM TRIFLUOROMETHANESULFONATE Usage And Synthesis

Uses

Hafnium trifluoromethanesulfonate is a recyclable catalyst for the mononitration of o-nitrotoluene. It serves as a catalyst for homogeneous methoxycarbonylation and hydrocarboxylation reactions of phenylacetylene. It is also used as a reactant for direct Friedel-Crafts reactions of chromene hemiacetals, aminomethylation reactions under Lewis acidic conditions and prins-type cyclization reactions. It is also involved in the direct polycondensation of lactic acid. Further, it is used in cationic benzylation reactions, chemoselective thioacetalization and transthioacetalization of carbonyl compounds.

Uses

Catalyst for:

  • Homogeneous methoxycarbonylation and hydrocarboxylation reactions of phenylacetylene
  • Direct Friedel-Crafts reactions of chromene hemiacetals
  • Aminomethylation reactions under Lewis acidic conditions
  • Prins-type cyclization reactions
  • Direct polycondensation of lactic acid
  • Cationic benzylation reactions
  • Chemoselective thioacetalization and transthioacetalization of carbonyl compounds

HAFNIUM TRIFLUOROMETHANESULFONATESupplier

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