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76089-77-5

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76089-77-5 Usage

Description

Cerium(III) Trifluoromethanesulfonate is a cerium salt of Trifluoromethanesulfonic acid (T790560), a strong acid that is known for its catalytic properties in various chemical reactions.

Uses

Used in Chemical Synthesis:
Cerium(III) Trifluoromethanesulfonate is used as a catalyst for esterification reactions, facilitating the formation of esters from acids and alcohols. Its strong acidic nature makes it a suitable catalyst for promoting esterification processes in the chemical synthesis industry.
Used in Organic Chemistry:
In the field of organic chemistry, Cerium(III) Trifluoromethanesulfonate is employed as a reagent and catalyst for various organic transformations, such as the synthesis of complex organic molecules and the modification of existing compounds. Its ability to act as a Lewis acid enhances its utility in these applications.
Used in Pharmaceutical Industry:
Cerium(III) Trifluoromethanesulfonate is utilized in the pharmaceutical industry for the synthesis of drug molecules and intermediates. Its catalytic properties enable the efficient production of desired compounds, contributing to the development of new medications and therapies.
Used in Material Science:
In material science, Cerium(III) Trifluoromethanesulfonate is applied in the synthesis of advanced materials, such as polymers, composites, and nanomaterials. Its role as a catalyst can help in the development of new materials with improved properties and applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 76089-77-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,0,8 and 9 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 76089-77:
(7*7)+(6*6)+(5*0)+(4*8)+(3*9)+(2*7)+(1*7)=165
165 % 10 = 5
So 76089-77-5 is a valid CAS Registry Number.
InChI:InChI=1/3CHF3O3S.Ce/c3*2-1(3,4)8(5,6)7;/h3*(H,5,6,7);/q;;;+3/p-3

76089-77-5 Well-known Company Product Price

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  • TCI America

  • (T1918)  Cerium(III) Trifluoromethanesulfonate  >90.0%(T)

  • 76089-77-5

  • 5g

  • 540.00CNY

  • Detail
  • TCI America

  • (T1918)  Cerium(III) Trifluoromethanesulfonate  >90.0%(T)

  • 76089-77-5

  • 25g

  • 1,790.00CNY

  • Detail
  • Alfa Aesar

  • (L20251)  Cerium(III) trifluoromethanesulfonate, 98%   

  • 76089-77-5

  • 5g

  • 683.0CNY

  • Detail
  • Alfa Aesar

  • (L20251)  Cerium(III) trifluoromethanesulfonate, 98%   

  • 76089-77-5

  • 25g

  • 2617.0CNY

  • Detail

76089-77-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Cerium(III) Triflate

1.2 Other means of identification

Product number -
Other names cerium(3+),trifluoromethanesulfonate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:76089-77-5 SDS

76089-77-5Relevant articles and documents

A general synthesis and crystal structure of 3Ce

Sofield, Chadwick D.,Andersen, Richard A.

, p. 271 - 276 (1995)

The preparation of 3Ce from Ce(OSO2CF3)3 and 2Mg is described and compared to published routes to other Cp3Ln(Ln=lanthanide) compounds.The title compound is monomeric in the solid state with three η5-bound cyclopentadienyl rings which show some unusual distortions while maintaining idealized C3h symmetry.The crystals are monoclinic, in the space group P21/n with the unit cell a 10.803(3) b 19.493(6) c 17.946(5) Angstroem, β 104.35(2) deg, Z=4.Anisotropic refinement of all heavy atoms with 361 parameters and 3420 reflections yielded R=4.62percent.Keywords: Cerium; Trivalent metallocene; Crystal structure

Process for the preparation of aryl ketones generating reduced amounts of toxic byproducts

-

Example 1, (2010/11/29)

An efficient, cost-effective method useful for the production of aryl ketones that minimizes the generation of toxic byproducts is disclosed. The method utilizes a metal triflate salt to catalyze the reaction between the carboxylic acid substrate and the aromatic substrate. The water generated by the reaction is collected and removed during the process.

Method for inhibiting perspiration

-

, (2008/06/13)

Method of inhibiting perspiration with antiperspirant compositions containing trivalent metal salts of trifluoromethanesulfonic acid of the formula: wherein Me is aluminum, lanthanum, cerium or didymium obtained by reacting trifluoromethanesulfonic acid with the appropriate metal carbonate or sulfide or by the exchange reaction of the appropriate metal sulfate with barium trifluoromethanesulfonate.

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