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136569-57-8

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136569-57-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 136569-57-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,5,6 and 9 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 136569-57:
(8*1)+(7*3)+(6*6)+(5*5)+(4*6)+(3*9)+(2*5)+(1*7)=158
158 % 10 = 8
So 136569-57-8 is a valid CAS Registry Number.

136569-57-8Downstream Products

136569-57-8Relevant articles and documents

Five-membered cyclopalladated complex containing bidentate phosphine ligands; Synthesis, characterization, and highly efficient Suzuki cross-coupling reactions

Sabounchei, Seyyed Javad,Ahmadi, Mohsen,Nasri, Zahra

, p. 411 - 423 (2013)

A nonsymmetric phosphorus ylide and its palladium(II) complex have been synthesized as potential catalytically active compounds. The reaction of 1 equiv nonsymmetric phosphorus ylide, Ph2PCH2PPh 2C(H)C(O)PhBr with [Pd(dppe)Cl2], followed by treatment with 2 equiv AgOTf led to [(dppe)Pd(Ph2PCH2PPh 2C(H)C(O)PhBr)](OSO2CF3)2, which contains a five-membered P,P chelate ring on one side and a five-membered P,C chelate ring on the other side. The palladium complex was synthesized and investigated by fourier transform infrared spectroscopy (FT-IR), UV-visible, multinuclear (1H, 31P and 19F) nuclear magnetic resonance (NMR), and electrospray ionisation-mass spectroscopic techniques. FT-IR and 31P NMR studies revealed that the phosphorus ylide is coordinated to palladium via the terminal phosphorus (Pc) of the ylide and methene group (CH). Suzuki reactions for varying aryl halides using the cyclopalladated complex as an efficient catalyst were performed. Various aryl halides were coupled with arylboronic acids in DMF, under air, in the presence of 0.001 mol% of the homogeneous catalyst to afford the corresponding cross-coupled products in good to excellent yields.

Triphenylene based metal-pyridine cages

Berton, Giacomo,Lorenzetto, Tommaso,Borsato, Giuseppe,Sgarbossa, Paolo,Santo, Claudio,Visentin, Fabiano,Fabris, Fabrizio,Scarso, Alessandro

supporting information, (2019/10/02)

C3-symmetric pyridine containing tris-benzyl-O-substituted hexahydroxytriphenylene derivatives were prepared and used in combination with square-planar Pd(II) and Pt(II) complexes for the self-assembly of molecular cages in solution. The formation of a trigonal bipyramid M3L2 cage was demonstrated by multinuclear NMR analyses and pseudo 2D DOSY experiments and supported by semi-empirical calculations.

Synthesis, characterization, thermal, electrochemical, and DFT studies of mononuclear cyclopalladated complexes containing bidentate phosphine ligands and their biological evaluation as antioxidant and antibacterial agents

Sabounchei, Seyyed Javad,Ahmadi, Mohsen,Nasri, Zahra,Shams, Esmaeil,Salehzadeh, Sadegh,Gholiee, Yasin,Karamian, Roya,Asadbegy, Mostafa,Samiee, Sepideh

, p. 159 - 175 (2013/06/05)

The non-symmetric phosphorus ylides and their Pd(II) complexes have been synthesized as potential antioxidant and antibacterial compounds and their structures were elucidated using a variety of physicochemical techniques. The reaction of 1 equiv non-symmetric phosphorus ylides, Ph2PCH 2PPh2C(H)C(O)PhX (X = Br (Y1), Cl (Y 2), NO2 (Y3), OCH3 (Y4)) with [Pd(dppe)Cl2] (M1), followed by treatment with 2 equiv AgOTf led to monomeric chelate complexes, [(dppe)Pd(Ph2PCH 2PPh2C(H)C(O)PhX)] (OSO2CF3) 2 (X = Br (C1), Cl (C2), NO2 (C 3), OCH3 (C4)), which contain a five-membered P,P chelate ring in one side and a five-membered P,C chelate ring in the other side. Palladium ion complexes were synthesized and investigated by cyclic voltammetry, FT-IR, UV-visible, multinuclear (1H, 31P and 19F) NMR, thermal analysis and ESI-mass spectroscopic studies. Some complexes and ligands have been studied by powder XRD and single crystal X-ray diffraction techniques. FT-IR and 31P NMR studies revealed that the ylides Y are coordinated to the metal ions via the terminal phosphorus (P c) of the ylides and methene group (CH). The proposed coordination geometry around the Pd atom in these complexes is defined as slightly distorted square planar by UV-Visible and DFT studies. Thermal stability of all complexes was also shown by TG/DTG methods. Furthermore, the electrochemical behavior of the complexes was investigated by cyclic voltammetry. The results indicate that all complexes are successfully synthesized from the initial ligands. All complexes were analyzed for their antioxidant properties by DPPH free radical scavenging assay. In addition, the antibacterial effects of the hexane-solved complexes were investigated by disc diffusion method against four Gram positive and negative bacteria. All complexes represented antibacterial activity against bacteria tested especially on Gram positive ones. A theoretical study on the structure, 1H and 31P NMR chemical shifts and the interaction energy between the Pd2+ ion and ligands dppe and ylide Y is also reported.

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