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124268-93-5

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124268-93-5 Usage

Chemical Properties

purple/red solid

Check Digit Verification of cas no

The CAS Registry Mumber 124268-93-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,2,6 and 8 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 124268-93:
(8*1)+(7*2)+(6*4)+(5*2)+(4*6)+(3*8)+(2*9)+(1*3)=125
125 % 10 = 5
So 124268-93-5 is a valid CAS Registry Number.

124268-93-5 Well-known Company Product Price

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  • Alfa Aesar

  • (44980)  Dibromo[1,1'-bis(diphenylphosphino)ferrocene]palladium(II), Pd 12.9%   

  • 124268-93-5

  • 1g

  • 1536.0CNY

  • Detail
  • Alfa Aesar

  • (44980)  Dibromo[1,1'-bis(diphenylphosphino)ferrocene]palladium(II), Pd 12.9%   

  • 124268-93-5

  • 5g

  • 6637.0CNY

  • Detail

124268-93-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name [1,1'-Bis(diphenylphosphino)ferrocene]palladium(II) bromide, Pd 12.9%

1.2 Other means of identification

Product number -
Other names {1,1'-bis(diphenylphosphino)ferrocene} palladium dibromide

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:124268-93-5 SDS

124268-93-5Relevant articles and documents

Synthesis, Characterization, and Reactivity of Palladium Fluoroenolate Complexes

Arlow, Sophie I.,Hartwig, John F.

supporting information, p. 16088 - 16091 (2017/11/22)

Cross-coupling reactions of aryl groups with α-fluoro carbonyl compounds catalyzed by palladium complexes have been reported, but palladium fluoroenolate intermediates relevant to such reactions have not been isolated or even detected previously. We report the synthesis, structural characterization, and reactivity of a series of C-bound arylpalladium fluoroenolate complexes ligated by monophosphines and bisphosphines. DPPF-ligated arylpalladium fluoroenolate complexes (DPPF = 1,1-bis(diphenylphosphino)-ferrocene) derived from a monofluoroester, a difluoroester, difluoroamides, and difluoroacetonitrile underwent reductive elimination in high yields. Reductive elimination was faster from complexes containing less electron-withdrawing fluoroenolate groups and longer Pd-C(enolate) bonds than from complexes containing more electron-withdrawing fluoroenolate groups and shorter Pd-C(enolate) bonds. The rates of reductive elimination from these C-bound fluoroenolate complexes were significantly faster than those of the analogous trifluoromethyl complexes.

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