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trans-bis(nitrato)bis(4-n-butylphenylamine)platinum(II) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1021689-96-2

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1021689-96-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1021689-96-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,1,6,8 and 9 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1021689-96:
(9*1)+(8*0)+(7*2)+(6*1)+(5*6)+(4*8)+(3*9)+(2*9)+(1*6)=142
142 % 10 = 2
So 1021689-96-2 is a valid CAS Registry Number.

1021689-96-2Downstream Products

1021689-96-2Relevant academic research and scientific papers

Synthesis and study of Pt(II)-aromatic amines complexes of the types cis- and trans-Pt(amine)2(NO3)2 and cis-Pt(amine)2(R(COO)2)

Rochon, Fernande D.,Massarweh, Gassan,Bonnier, Catherine

, p. 1437 - 1446 (2008/10/09)

Complexes of the types cis- and trans-Pt(amine)2(NO3)2 with amines containing a phenyl group were synthesized and studied mainly by IR and multinuclear magnetic resonance spectroscopies. The cis complexes could be synthesized pure only with the amines of the type Ph-R-NH2 (R = alkyl), while pure trans compounds were synthesized with all the studied amines. In 195Pt NMR spectroscopy, the dinitrato complexes of the amines Ph-R-NH2 were observed around -1700 ppm for the cis isomers and at about -1580 for the trans complexes. For the other amines, where a phenyl ring is directly attached to the amino group, the signals were observed at lower fields, -1528 ppm for cis-Pt(PhNH2)(NO3)2 and around -1450 ppm for all the trans isomers. There is a linear relationship between the δ(Pt) of the Pt(amine)2(NO3)2 complexes and the pKa of the protonated amines. The coupling constants 2J(195Pt-1HN) are larger in the cis compounds (ave. 76 Hz) than in the trans isomers (ave. 63 Hz). The complexes cis-Pt(amine)2(R(COO)2) with bidentate dicarboxylato ligands were also synthesized and characterized mainly by IR spectroscopy. The compounds apparently decompose in DMF and are too insoluble in other solvents for solution studies.

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