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57384-29-9

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57384-29-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57384-29-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,3,8 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 57384-29:
(7*5)+(6*7)+(5*3)+(4*8)+(3*4)+(2*2)+(1*9)=149
149 % 10 = 9
So 57384-29-9 is a valid CAS Registry Number.

57384-29-9Downstream Products

57384-29-9Relevant articles and documents

Thermodynamic study of lanthanide(iii) complexes with bifunctional monophosphinic acid analogues of H4dota and comparative kinetic study of yttrium(iii) complexes

Foersterova, Michaela,Svobodova, Ivona,Lubal, Pemysl,Taborsky, Petr,Kotek, Jan,Hermann, Petr,Luke, Ivan

, p. 535 - 549 (2007)

New bifunctional H4dota-like ligands with three acetic acid and one phosphinic acid pendant arms and propionate (H5do3ap PrA) or 4-aminobenzyl (H4do3apABn) reactive groups bound to the phosphorus atom were investigated. Potentiometric studies showed that the ligands have a similar basicity to the parent H4dota and the stability constants of their complexes with sodium(i) and selected lanthanide(iii) ions are also similar. Formation and acid-assisted decomplexation kinetics of yttrium(iii) complexes with a series of H 4dota-like ligands (H4dota and its phosphinic/phosphonic acid analogues) were studied and the reactions are sensitive to a slight modification of the ligand structure. The (2-carboxyethyl)phosphinic acid derivative H5do3apPrA and the phosphonic acid ligand H5do3ap form complexes faster than H4dota. The most kinetically inert complex is that with H4do3apABn. Rates of complexation and decomplexation can depend on the ability to transfer proton(s) outside/inside the complex cavity and, therefore, on the hydrophobicity of the ligands. The results demonstrate that the new bifunctional ligands are suitable for labelling biomolecules with yttrium(iii) radioisotopes for utilization in nuclear medicine. The Royal Society of Chemistry 2007.

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