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AuCl2(P(C6H5)3)(C6F5) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

37822-98-3

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37822-98-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 37822-98-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,8,2 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 37822-98:
(7*3)+(6*7)+(5*8)+(4*2)+(3*2)+(2*9)+(1*8)=143
143 % 10 = 3
So 37822-98-3 is a valid CAS Registry Number.

37822-98-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name cis-[AuIII(C6F5)Cl2(PPh3)]

1.2 Other means of identification

Product number -
Other names cis-dichloro(pentafluorophenyl)(triphenylphosphine)gold(III)

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:37822-98-3 SDS

37822-98-3Relevant academic research and scientific papers

A neutral Gold(III)-Boron transmetalation

Hofer, Manuel,Gomez-Bengoa, Enrique,Nevado, Cristina

supporting information, p. 1328 - 1332 (2014/04/17)

The occurrence of direct transmetalation between gold(III) and boron species during gold-catalyzed cross-coupling reactions has recently become the subject of intense discussion. In this work, we investigate the transmetalation reaction between discrete, stable gold(III) complexes and boron reagents. Interestingly, electron-rich arylboronic acids remain unreactive under neutral conditions, whereas electron-deficient species undergo transmetalation in a highly efficient manner.

Cross-coupling of arene-gold(III) complexes

Hofer, Manuel,Nevado, Cristina

, p. 5751 - 5757 (2013/07/11)

The reactivity of electron-deficient arene-gold(III) complexes toward nucleophilic aromatic and heteroaromatic counterparts has been studied. 1-Methylindole proved to be the best reaction partner while trimethoxybenzenes did not react. The ancillary ligand on gold also influenced the reactivity in the order PPh3>PtBu3>IPr. An oxidative cross-coupling starting from the corresponding gold(I) complexes in presence of hypervalent iodide oxidants was also studied.

Unexpected outcomes of the oxidation of (pentafluorophenyl) triphenylphosphanegold(I)

Hofer, Manuel,Nevado, Cristina

, p. 1338 - 1341 (2012/05/20)

Redox gold(I)/gold(III) catalytic cycles have been proposed as the productive mechanistic manifold in a number of gold mediated C-C and C-X bond forming reactions. These transformations rely on the use of stoichiometric oxidants such as iodonium salts and

DIHALO PENTAFLUOROPHENYL TETRAHYDROTHIOPHEN GOLD(III) COMPLEXES, THEIR PREPARATION AND REACTIONS

Uson, R.,Laguna, A.,Bergareche, B.

, p. 411 - 416 (2007/10/02)

The complex Au(C6F5)(tht) undergoes oxidative addition when treated in solution with halogens, to give Au(C6F5)X(tht) (X=Cl, Br or I).The tetrahydrothiophen ligand of the latter can be displaced by neutral or anionic ligands to give, respectively, the neu

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