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[RhHCl(PPh3){κ3-P,Si,P′-SiPh(NCH2PPh2)2-C6H4}] is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1541882-36-3

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1541882-36-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1541882-36-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,4,1,8,8 and 2 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1541882-36:
(9*1)+(8*5)+(7*4)+(6*1)+(5*8)+(4*8)+(3*2)+(2*3)+(1*6)=173
173 % 10 = 3
So 1541882-36-3 is a valid CAS Registry Number.

1541882-36-3Relevant 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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