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dichlorido{N-[2-(diphenylphosphanyl)benzylidene]-2-methylaniline}-palladium(II) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1433901-83-7

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1433901-83-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1433901-83-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,3,3,9,0 and 1 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1433901-83:
(9*1)+(8*4)+(7*3)+(6*3)+(5*9)+(4*0)+(3*1)+(2*8)+(1*3)=147
147 % 10 = 7
So 1433901-83-7 is a valid CAS Registry Number.

1433901-83-7Downstream Products

1433901-83-7Relevant academic research and scientific papers

Iminophosphine palladium(II) complexes: Synthesis, characterization, and application in Heck cross-coupling reaction of aryl bromides

Yilmaz, Mustafa Kemal,Guezel, Bilgehan

, p. 529 - 536 (2014/07/07)

Palladium(II) complexes containing phosphorus and nitrogen donor atoms (iminophosphine), dichlorido{N-[2-(diphenylphosphino)benzylidene]-2- trifluoromethylaniline}palladium(II) 1, dichlorido{N-[2-(diphenylphosphino) benzylidene]-3-trifluoromethylaniline}palladium(II) 2, dichlorido{N-[2- (diphenylphosphino)benzylidene]-2-methylaniline}palladium(II) 3, dichlorido{N-[2-(diphenylphosphino)benzylidene]-3-methylaniline}palladium(II) 4 have been successfully synthesized and fully characterized by FT-IR and NMR (1H, 31P, 19F, and 13C) spectroscopy techniques. These complexes were first step tested in the reaction of bromobenzene and styrene to determine the optimal coupling reaction conditions and then successfully applied as catalysts for Heck cross-coupling reactions of activated and deactivated aryl bromides with styrene derivatives and several acrylates. Copyright

Dichlorido{N-[2-(diphenylphosphanyl)benzylidene]-2-methylaniline} palladium(II) acetonitrile monosolvate

Motswainyana, William M.,Onani, Martin O.,Jacobs, Jeroen,Van Meervelt, Luc

, p. 209 - 211 (2013/04/24)

The title imino-phosphine compound, [PdCl2(C26H 22NP)]·CH3CN, was prepared by reaction of N-[2-(diphenylphosphanyl)benzylidene]-2-methylaniline with dichlorido(cycloocta- 1,5-diene)palladium(II) in dry CH2Cl2. The PdII cation is coordinated by the P and N atoms of the bidentate chelating ligand and by two chloride anions, generating a distorted square-planar coordination geometry. There is a detectable trans influence for the chloride ligands. The methyl group present in this structure has an influence on the crystal packing. Copyright

Imino-phosphine palladium(II) and platinum(II) complexes: Synthesis, molecular structures and evaluation as antitumor agents

Motswainyana, William M.,Onani, Martin O.,Madiehe, Abram M.,Saibu, Morounke,Thovhogi, Ntevheleni,Lalancette, Roger A.

, p. 112 - 118 (2013/10/22)

The imino-phosphine ligands L1 and L2 were prepared via condensation reaction of 2-(diphenylphosphino)benzaldehyde with substituted anilines and obtained in very good yields. An equimolar reaction of L1 and L2 with either PdCl2(cod) or PtCl2(cod) gave new palladium(II) and platinum(II) complexes 1-4. The compounds were characterized by elemental analysis, IR, 1H and 31P NMR spectroscopy. The molecular structures of 2, 3 and 4 were confirmed by X-ray crystallography. All the three molecular structures crystallized in monoclinic C2/c space system. The coordination geometry around the palladium and platinum atoms in respective structures exhibited distorted square planar geometry at the metal centers. The complexes were evaluated in vitro for their cytotoxic activity against human breast (MCF-7) and human colon (HT-29) cancer cells, and they exhibited growth inhibitory activities and selectivity that were superior to the standard compound cisplatin.

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