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[Ph2P(ferrocene-1,1'-diyl)C(O)(2-pyridyl)] is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1235551-40-2

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1235551-40-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1235551-40-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,5,5,5 and 1 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1235551-40:
(9*1)+(8*2)+(7*3)+(6*5)+(5*5)+(4*5)+(3*1)+(2*4)+(1*0)=132
132 % 10 = 2
So 1235551-40-2 is a valid CAS Registry Number.

1235551-40-2Downstream Products

1235551-40-2Relevant academic research and scientific papers

Synthesis, structural characterization, and catalytic evaluation of palladium complexes with homologous ferrocene-based pyridylphosphine ligands

Stepnicka, Petr,Schulz, Jiri,Klemann, Thorsten,Siemeling, Ulrich,Cisarova, Ivana

, p. 3187 - 3200 (2010/12/24)

A ferrocene-based phosphinopyridine, Ph2PfcPy (1; fc = ferrocene-1,1'-diyl, Py = 2-pyridyl), was newly synthesized by Negishi coupling of Ph2PfcZnCl with PyBr. Its homologous compound Ph2PfcCH 2Py (2) was obtained by reductive dehydroxylation of Ph 2PfcCH(OH)Py (4), the latter resulting via reaction of in situ generated Ph2PfcLi with PyCHO. Depending on the stoichiometry, compounds 1 and 2 react with [PdCl2(cod)] (cod = η2:η2- cycloocta-1,5-diene) to give P,N-chelate and bis-phosphine complexes, [PdCl 2(L-?2P,N)] (5, L = 1;6, L = 2) and [PdCl 2(L-?P)2] (7, L = 1;8, L = 2), respectively. Analogously, [(LNC)PdCl]2 or [(LNC)Pd(MeCN) 2]ClO4 (LNC = [(2-dimethylamino-?N)methyl] phenyl-?C1) react with 1 and 2 to afford complexes featuring these compounds as P-monodentate ligands ([(LNC)PdCl(L-?P)]: 9, L = 1;10, L = 2) or P,N-chelating donors ([(LNC)Pd(L-?2P,N)]ClO 4: 11, L = 1;12, L = 2), respectively. With the exception of compound 9, which undergoes self-ionization in solution, all complexes are defined air-stable solids and were characterized by elemental analysis and conventional spectroscopic methods (multinuclear NMR, IR, and MS). The crystal structures of 4, 5, 7 3 CH2Cl2, 8, 11, and 12 were determined by X-ray crystallography, revealing structural differences resulting from a more flexible geometry of the methylene-spaced ligand 2. The catalytic potential of the Pd complexes 5 and 6 and their in situ generated counterparts (Pd(OAc) 2/L, L = 1, 2) was studied in Suzuki-Miyaura cross-coupling of 4-bromotoluene (13) with phenylboronic acid and in cyanation of the same substrate with K4[Fe-(CN)6]. The results were compared with those obtained under identical conditions with analogous catalysts based on the related donor-symmetric ligand 1,1'-bis(diphenylphosphino)ferrocene.

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