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(diphenyl-tert-butylphosphine)2PdCl2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

34408-87-2

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34408-87-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34408-87-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,4,0 and 8 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 34408-87:
(7*3)+(6*4)+(5*4)+(4*0)+(3*8)+(2*8)+(1*7)=112
112 % 10 = 2
So 34408-87-2 is a valid CAS Registry Number.

34408-87-2Downstream Products

34408-87-2Relevant academic research and scientific papers

Anticancer metallopharmaceutical agents based on mixed-ligand palladium(II) complexes with dithiocarbamates and tertiary organophosphine ligands

Khan, Hizbullah,Badshah, Amin,Said, Muhammad,Murtaza, Ghulam,Ahmad, Jamil,Jean-Claude, Bertrand J.,Todorova, Margarita,Butler, Ian S.

, p. 387 - 395 (2013)

Mixed-ligand palladium(II) complexes of the type [(DT)Pd(PR 3)Cl], where DT = diethyldithiocarbamate (1), dibutyldithiocarbamate (2,3), dipropyldithiocarbamate (4,5), bis(2-methoxyethyl)dithiocarbamate; PR3 = benzyldiphenylphosphine (1,4), diphenyl-o-tolylphosphine (2), diphenyl-t-butylphosphine (3), P-chlorodiphenylphosphine (5) and triphenylphosphine (6), have been synthesized and characterized by elemental analyses and FT-IR, Raman and multinuclear NMR spectroscopy. The structures of compounds 1 and 2 were determined by single-crystal X-ray diffraction (XRD) measurements and these analyses showed that the complexes have pseudo square-planar geometry around the Pd(II) and that the dithiocarbamate ligand is bound in a bidentate fashion, while the remaining two positions are occupied by a tertiary organophosphine and a chloride ligand. The anticancer studies showed that the Pd(II) complexes are highly active against cisplatin-resistant DU145 human prostate carcinoma (HTB-81) cells with the highest activity shown by compound 6 (IC50 = 2.12 μm). The redox behavior and ds-DNA-denaturing ability of the complexes were studied by cyclic voltammetry and two reduction and one oxidation waves were observed. The decrease in the reduction peak currents illustrated the consumption of the mixed-ligand drug by the DNA molecule. Copyright

Synthesis, structural characterization and biological screening of heteroleptic palladium(II) complexes

Khan, Hizbullah,Badshah, Amin,Said, Muhammad,Murtaza, Ghulam,Sirajuddin, Muhammad,Ahmad, Jamil,Butler, Ian S.

, p. 176 - 182 (2016/05/09)

Heteroleptic palladium(II) complexes of the type formula [(DTC)(Pd)(PR3)Cl], where DTC = bis(2-ethylhexyl)dithiocarbamate (1, 8, 9, 10), bis(2-methoxyethyl)dithiocarbamate (2), di-n-decyldithiocarbamate (3, 6), di-n-hexyldithiocarbamate (4, 7), bis(2-methylbutyl)dithiocarbamte (5); PR3 = diphenyl-t-butylphosphine (1), diphenyl-n-propylphosphine (2), triphenylphosphine (3, 4, 5, 10), diphenyl-p-tolylphosphine (6, 7, 8), diphenylbenzylphosphine (9); have been synthesized and characterized by FTIR, Raman, multinuclear and multinuclear NMR (1H, 13C, 31P) spectroscopy and elemental analyses. The structures of complexes (1 and 2) were determined by single-crystal X-ray diffraction. The geometries around the metal centers are pseudo square-planar. The new complexes exhibit moderate anticancer and antibacterial activity.

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