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167416-28-6

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  • Factory Price OLED 99% 167416-28-6 (R)-(-)-1-[(S)-2-Dicyclohexylphosphino)ferrocenyl]ethyldicyclohexylphosphine Manufacturer

    Cas No: 167416-28-6

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167416-28-6 Usage

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Ligand for Pd-catalyzed C-N cross-coupling Ligand for Rh-catalyzed C-N cross-coupling Ligand for Pd-catalyzed asymmetric synthesis of (S)-QUINAP via dynamic kinetic resolution Ligand for Ni-catalyzed monoarylation of ammonia

General Description

sold in collaboration with Solvias AG

Check Digit Verification of cas no

The CAS Registry Mumber 167416-28-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,7,4,1 and 6 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 167416-28:
(8*1)+(7*6)+(6*7)+(5*4)+(4*1)+(3*6)+(2*2)+(1*8)=146
146 % 10 = 6
So 167416-28-6 is a valid CAS Registry Number.
InChI:InChI=1/C31H51P2.C5H5.Fe/c1-25(32(26-15-6-2-7-16-26)27-17-8-3-9-18-27)30-23-14-24-31(30)33(28-19-10-4-11-20-28)29-21-12-5-13-22-29;1-2-4-5-3-1;/h14,23-29H,2-13,15-22H2,1H3;1-5H;/t25-;;/m1../s1

167416-28-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-1-[(1S)-2-(DICYCLOHEXYLPHOSPHINO)FERROCENYL]ETHYLDICYCLOHEXYLPHOSPHINE

1.2 Other means of identification

Product number -
Other names (R)-(-)-1-[(S)-2-Dicyclohexylphosphino)ferrocenyl]ethyldicyclohexylphosphine

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

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More Details:167416-28-6 SDS

167416-28-6Downstream Products

167416-28-6Relevant articles and documents

Rhodium-Catalyzed Asymmetric Allylation of Malononitriles as Masked Acyl Cyanide with Allenes: Efficient Access to β,γ-Unsaturated Carbonyls

Grugel, Christian P.,Breit, Bernhard

supporting information, p. 15223 - 15226 (2018/09/25)

A rhodium-catalyzed regio- and enantioselective intermolecular allylation of malononitriles as masked acyl cyanides (MAC) with terminal and symmetrical internal allenes is reported. A RhI/Josiphos catalytic system combined with subsequent oxidative degradation of the primary adducts enables a straightforward access to α-branched, β,γ-unsaturated carbonyl compounds. The present protocol exhibits perfect atom economy in the allylation step and is characterized by a great functional group compatibility. Furthermore, the use of α-substituted malononitriles allowed for the construction of all-carbon quaternary centers.

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