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[Pt(oxalate)(bis(diphenylphosphino)methane)] is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

103636-92-6

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103636-92-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103636-92-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,6,3 and 6 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 103636-92:
(8*1)+(7*0)+(6*3)+(5*6)+(4*3)+(3*6)+(2*9)+(1*2)=106
106 % 10 = 6
So 103636-92-6 is a valid CAS Registry Number.

103636-92-6Relevant articles and documents

Oxidative degradation of the ascorbate anion in the presence of platinum and palladium. Formation and structures of platinum and palladium oxalate complexes

Arendse, Malcolm J.,Anderson, Gordon K.,Rath, Nigam P.

, p. 2495 - 2503 (2008/10/08)

The reactions of [Pt(NO3)2(dppm)] (dppm = bis(diphenylphosphino)methane) and cis-[Pt(NO3)2(PEt3)2] with sodium ascorbate are described. Complexes containing O,O-coordinated ascorbate ligand

Photochemical reactions of diphosphineplatinum(II) oxalate complexes

Anderson, Gordon K.,Lumetta, Gregg J.,Siria, Jeffrey W.

, p. 253 - 259 (2007/10/02)

Irradiation at 254 nm of CH3CN/C6H6 or PhCn solutions of produces 2 equiv. of CO2, and in the presence of PhCl or PhI yields .With CO or PhCCPh the products are or CPh)(dppe)>, but in the latter case extended photolysis yields CPh)(dppe)>.Photolysis in the presence of H2 gives a mixture of the + and + cations.Simple elimination of CO2 does not occur in all cases, as illustrated by the formation of when is photolyzed in the presence of methanol.Photochemical reactions of the related complexes (L2 = dppm, dcpe) are also described.

REACTIONS OF DIPHOSPHINEPLATINUM(II) OXALATE COMPLEXES WITH PHENYLACETYLENE. FORMATION OF PHENYLALKYNYLPLATINUM COMPLEXES

Anderson, Gordon K.,Lumetta, Gregg J.

, p. 257 - 264 (2007/10/02)

reacts thermally with PhCCH to produce CPh)2(dppe)>, which has been prepared by alternative routes.Similar treatment of initially produces CPh)2(dpmm)>, which rearranges to give cis,cis-CPh)4(μ-dppm)2>.Reaction of with PhCCH/KOH/18-crown-6, or with (PhCC)SnMe3, gives CPh)2(dpmm)>, which may be converted to the cis,cis-dimer by addition of oxalic acid.Ultraviolet irradiation or refluxing with a trace amount of dppm converts CPh)2(dppm)> to trans,trans-CPh)4(μ-dppm)2>, but the cis,cis-dimer is stable under these conditions. (L = PPh3, PEt3) complexes also react thermally with PhCCH to yield CPh)2L2> species.

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