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144026-79-9

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  • China Largest factory Manufacturer Supply Scandium trifluoromethanesulfonate CAS 144026-79-9

    Cas No: 144026-79-9

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144026-79-9 Usage

Description

Scandium trifluoromethanesulfonate, commonly called Scandium(III) triflate, is a chemical compound with formula Sc(SO3CF3)3, a salt consisting of scandium cations Sc3+ and triflate SO3CF3? anions.Scandium(III) triflate is an extremely active, efficient, recoverable and reusable acylation catalyst. Its an important catalyst for the Friedel-Crafts acylation, Diels-Alder reactions and other carbon-carbon bond-forming reactions. It also stereochemically catalyzes the radical polymerization of acrylates. Scandium(III) triflate complex of (4′S,5′S)-2,6-bis[4′-(triisopropylsilyl)oxymethyl-5′-phenyl-1′,3′-oxazolin-2′-yl]pyridine has been employed as catalyst for the asymmetric Friedel-Crafts reaction between substituted indoles and methyl (E)-2-oxo-4-aryl-3-butenoates.

Chemical Properties

White powder

Uses

Different sources of media describe the Uses of 144026-79-9 differently. You can refer to the following data:
1. Scandium(III) trifluoromethanesulfonate is widely used as a catalyst in hydrothiolation, selective two-electron reduction of oxygen by ferrocene derivatives and vinylogous Fridel-crafts alkylation of indoles and pyrrole in water. It is involved in the Mukaiyama aldol addition and stereochemically catalyzes the radical polymerization of acrylates. It acts as a Lewis acid catalyst and used in the synthesis of bullvalone via a stabilized sulfur ylide.
2. Scandium Triflate is an important catalyst used in Friedel-Crafts acylation, Baylis-Hillman reaction and other carbon-carbon bond forming reactions.

Application

Scandium(III) triflate was used as a catalyst in:Hydrothiolation reaction of aromatic and aliphatic thiols.Selective two-electron reduction of O2 by ferrocene derivatives.Vinylogous Friedel-Crafts alkylation of indoles and pyrroles in water.Synthesis of β-cyanoketones.Combination with triethylsilane to reductively open functionalized pyranoside rings.The key steps of synthesis of bullvalone via a stabilized sulfur ylide.

Reactions

Water tolerant Lewis acid. Commonly used in a range of Lewis acid catalyzed reactions. Efficient metal source for Lewis acid catalyzed asymmetric reactions. Catalyzes Friedel-Crafts alkylation, acylation and related reactions. Catalyzes various domino- and multi-component processes. Catalyzes electrophilic additions of alpha-diazoesters with ketones. Catalyzes carbon insertion reactions.

General Description

Scandium(III) triflate is an extremely active, efficient, recoverable and reusable acylation catalyst. Its an important catalyst for the Friedel-Crafts acylation, Diels-Alder reactions and other carbon-carbon bond-forming reactions. It also stereochemically catalyzes the radical polymerization of acrylates. Scandium(III) triflate complex of (4′S,5′S)-2,6-bis[4′-(triisopropylsilyl)oxymethyl-5′-phenyl-1′,3′-oxazolin-2′-yl]pyridine has been employed as catalyst for the asymmetric Friedel-Crafts reaction between substituted indoles and methyl (E)-2-oxo-4-aryl-3-butenoates.

Check Digit Verification of cas no

The CAS Registry Mumber 144026-79-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,0,2 and 6 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 144026-79:
(8*1)+(7*4)+(6*4)+(5*0)+(4*2)+(3*6)+(2*7)+(1*9)=109
109 % 10 = 9
So 144026-79-9 is a valid CAS Registry Number.

144026-79-9 Well-known Company Product Price

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  • (Code)Product description
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  • Detail
  • TCI America

  • (T1663)  Scandium(III) Trifluoromethanesulfonate  >98.0%(T)

  • 144026-79-9

  • 1g

  • 650.00CNY

  • Detail
  • TCI America

  • (T1663)  Scandium(III) Trifluoromethanesulfonate  >98.0%(T)

  • 144026-79-9

  • 5g

  • 1,990.00CNY

  • Detail
  • Alfa Aesar

  • (40566)  Scandium(III) trifluoromethanesulfonate, 98%   

  • 144026-79-9

  • 250mg

  • 257.0CNY

  • Detail
  • Alfa Aesar

  • (40566)  Scandium(III) trifluoromethanesulfonate, 98%   

  • 144026-79-9

  • 1g

  • 687.0CNY

  • Detail
  • Alfa Aesar

  • (40566)  Scandium(III) trifluoromethanesulfonate, 98%   

  • 144026-79-9

  • 5g

  • 2640.0CNY

  • Detail
  • Aldrich

  • (483354)  Scandium(III)triflate  99.995% trace metals basis

  • 144026-79-9

  • 483354-1G

  • 1,404.00CNY

  • Detail
  • Aldrich

  • (418218)  Scandium(III)triflate  99%

  • 144026-79-9

  • 418218-250MG

  • 334.62CNY

  • Detail
  • Aldrich

  • (418218)  Scandium(III)triflate  99%

  • 144026-79-9

  • 418218-1G

  • 643.50CNY

  • Detail
  • Aldrich

  • (418218)  Scandium(III)triflate  99%

  • 144026-79-9

  • 418218-5G

  • 2,496.78CNY

  • Detail

144026-79-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name Scandium trifluoromethanesulfonate

1.2 Other means of identification

Product number -
Other names Trifluoromethanesulfonic Acid Scandium(III) Salt

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:144026-79-9 SDS

144026-79-9Upstream product

144026-79-9Downstream Products

144026-79-9Related news

Scandium trifluoromethanesulfonate (cas 144026-79-9) as Catalyst in the Hydrogen/Deuterium Exchange of 1,3,5-Trimethoxybenzene: Evidence for a Direct Interaction of Scandium with the Aromatic Ring07/11/2019

Scandium trifluoromethanesulfonate in CD3OD is a very active catalyst for hydrogen/deuterium exchange at the aromatic nucleus of 1,3,5-trimethoxybenzene. The very low proticity of the system, spectrophotometric evidence, and easy iodination of the substrate point to the formation of a transient ...detailed

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