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Zn(2+)*C19H17N4O3(1-)*O2CC6H4NO2(1-) = [Zn(C19H17N4O3)(O2CC6H4NO2)] is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

180680-53-9

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180680-53-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 180680-53-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,0,6,8 and 0 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 180680-53:
(8*1)+(7*8)+(6*0)+(5*6)+(4*8)+(3*0)+(2*5)+(1*3)=139
139 % 10 = 9
So 180680-53-9 is a valid CAS Registry Number.

180680-53-9Downstream Products

180680-53-9Relevant academic research and scientific papers

Zinc(II) complexes of tripodal ligands providing phenolate and pyridine donors: Formation, structure and hydrolytic activity

Adams, Harry,Bailey, Neil A.,Fenton, David E.,He, Qing-Yu

, p. 2857 - 2865 (1996)

A group of zinc(II) complexes derived from tri- and tetra-dentate proligands bearing pyridyl and phenolic arms have been prepared and characterised. Potentiometric titrations suggested that a stepwise complexation initially to the pendant OH, and then to pendant O- occurred. The crystal structures of [Zn2L32][ClO4]2 (L3 = 2-{bis[2-(2-pyridyl)ethyl]aminomethyl}phenolate) and [Zn2L62][Zn(NCS)4]·0.5H 2O (L6 = 2-{bis[2-(2-pyridyl)ethyl]aminomethyl}-4-nitrophenolate) reveal that both complexes are dimers in the solid state; the co-ordination geometries around zinc(II) can be best described as distorted square pyramidal with one pyridyl nitrogen atom, one tertiary nitrogen atom and two phenolic oxygen atoms forming the basal plane and a pyridyl nitrogen atom in the axial position. The interzinc separations are 3.284 A and 3.274 A respectively. The crystal structure of [Zn L72] (L7 = 4-nitro-2-{[2-(2-pyridyl)ethyl]aminomethyl}phenolate) reveals an octahedral complex with the zinc atom on a symmetry centre. The complexes [Zn2L32][ClO4]2 and [Zn2L62][BPh4]2, promote the hydrolysis of tris(4-nitrophenyl) phosphate; the former also has a small activity in the hydrolysis of bis(4-nitrophenyl) phosphate.

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