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Zinc trifluoromethanesulfonate

Names

[ CAS No. ]:
54010-75-2

[ Name ]:
Zinc trifluoromethanesulfonate

[Synonym ]:
Methanesulfonic acid, 1,1,1-trifluoro-, zinc salt, hydrate (2:1:1)
EINECS 258-922-6
Trifluoromethanesulfonic acid zinc salt
zinc,trifluoromethanesulfonate
MFCD00013229
Zinc(II) Trifluoromethanesulfonate
Zinc trifluoromethanesulfonate hydrate (1:2:1)
Trifluoromethanesulfonic acid zinc salt hydrate
Zinc(II) Triflate
Trifluoromethanesulfonic Acid Zinc(II) Salt
Zinc triflate hydrate
Zinc triflate

Chemical & Physical Properties

[ Density]:
4.43

[ Boiling Point ]:
162ºC at 760 mmHg

[ Melting Point ]:
≥300 °C(lit.)

[ Molecular Formula ]:
C2F6O6S2Zn

[ Molecular Weight ]:
381.563

[ Exact Mass ]:
379.843750

[ PSA ]:
131.16000

[ LogP ]:
2.26190

[ Storage condition ]:
Refrigerator

MSDS

Safety Information

[ Symbol ]:

GHS05

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H314

[ Precautionary Statements ]:
P280-P305 + P351 + P338-P310

[ Personal Protective Equipment ]:
Eyeshields;Faceshields;full-face particle respirator type N100 (US);Gloves;respirator cartridge type N100 (US);type P1 (EN143) respirator filter;type P3 (EN 143) respirator cartridges

[ Hazard Codes ]:
C: Corrosive;

[ Risk Phrases ]:
R34

[ Safety Phrases ]:
S26-S36/37/39-S45

[ RIDADR ]:
UN 3261 8/PG 2

[ WGK Germany ]:
3

[ Packaging Group ]:
II

[ Hazard Class ]:
8

[ HS Code ]:
2904909090

Synthetic Route

Precursor & DownStream

Customs

[ HS Code ]: 2904909090

[ Summary ]:
HS:2904909090 sulphonated, nitrated or nitrosated derivatives of hydrocarbons, whether or not halogenated VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0%

Articles

In(III)/PhCO2H binary acid catalyzed tandem [2 + 2] cycloaddition and Nazarov reaction between alkynes and acetals.

Org. Lett. 15(17) , 4496-9, (2013)

A facile tandem [2 + 2] cycloaddition and Nazarov reaction has been developed. The combination of In(OTf)3 and benzoic acid was found to synergistically promote the coupling of alkynes and acetals to ...

The synthesis of 3,5,6,7-tetrasubstituted isoxazolo[4,5-b]pyridines and an evaluation of their in vitro antiproliferative activity.

Adv. Clin. Exp. Med. 21(5) , 563-71, (2012)

Derivatives of isoxazolopyridines exhibit diverse biological activity. One method of synthesizing isoxazolo[4,5-b]pyridines is Friedlander condensation.To establish the conditions necessary for conven...

Michael addition/pericyclization/rearrangement--a multicomponent strategy for the synthesis of substituted resorcinols.

Org. Biomol. Chem. 10(31) , 6388-94, (2012)

The combination of methyl 3,7-dioxo-2-diazo-4-octenoate from the zinc triflate catalyzed Mukaiyama-Michael reaction of methyl 3-tert-butylsilyloxy-2-diazobutenoate and 4-methoxy-3-buten-2-one with Mic...


More Articles


Related Compounds

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