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[RhH(S2CNEt2){SiPh(NCH2PPh2)2C6H4}] is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1541151-53-4

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1541151-53-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1541151-53-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,4,1,1,5 and 1 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1541151-53:
(9*1)+(8*5)+(7*4)+(6*1)+(5*1)+(4*5)+(3*1)+(2*5)+(1*3)=124
124 % 10 = 4
So 1541151-53-4 is a valid CAS Registry Number.

1541151-53-4Downstream Products

1541151-53-4Relevant academic research and scientific papers

N-heterocyclic silyl pincer ligands

Dixon, Lily S. H.,Hill, Anthony F.,Sinha, Arup,Ward, Jas S.

, p. 653 - 658 (2014/03/21)

The reaction of 1,2-C6H4(NHCH2PPh 2)2 with chlorosilanes Cl2SiHR (R = Ph, Cl) affords the benzosiladiazoles RHSi(NCH2PPh2) 2C6H4 (R = Ph, 1; Cl, 2). The phenyl derivative 1 undergoes chelate-assisted Si-H activation with [RuPhCl(CO)(PPh 3)2] and [RhCl(PPh3)3] to afford the structurally characterized silyl pincer complexes [RuCl(CO)(PPh 3){κ3-P,Si,P′-SiPh(NCH2PPh 2)2C6H4}] (3) and [RhHCl(PPh 3){κ3-P,Si,P′-SiPh(NCH2PPh 2)2C6H4}] (4). The reaction of 4 with [Et2NH2][S2CNEt2] affords the complex [RhH(S2CNEt2){κ3-P,Si,P′- SiPh(NCH2PPh2)2C6H4}] (5), structural data for which demonstrate a pronounced trans influence for the σ-silyl donor.

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