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copper(II) bis-dibenzyldithiocarbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

15683-27-9

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15683-27-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15683-27-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,6,8 and 3 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 15683-27:
(7*1)+(6*5)+(5*6)+(4*8)+(3*3)+(2*2)+(1*7)=119
119 % 10 = 9
So 15683-27-9 is a valid CAS Registry Number.

15683-27-9Downstream Products

15683-27-9Relevant academic research and scientific papers

Electron Spin Resonance Study of Some Copper(II) Dithiocarbamates and their Mixed-ligand Complexes

Newton, William J.,Tabner, Brian J.

, p. 466 - 471 (1981)

The e.s.r. spectra of seven copper(II) dithiocarbamates have been recorded in chloroform-ethanol mixtures at room temperature and at 113 K.It has been found that the addition of a range of salts to these dithiocarbamates destroys the complex forming a mixed-ligand complex, , with a new e.s.r. spectrum.When X is Cl or Br the additional interaction of the unpaired electron with a single halogen nucleus is observed.The complex forms a dipole-dipole coupled dimer and a computer simulation of the ΔMs = 2 absorption of this dimer has been obtained.

KINETICS AND MECHANISM OF FORMATION OF COPPER (II) DITHIOCARBAMATES IN ACETONITRILE.

Maletin,Verkhovlyuk,Sheka

, p. 1 - 5 (2008/10/08)

Kinetics of formation of copper (II) bis-dithiocarbamates in a system, containing copper acetate, diethyl- or dibenzylamine, and carbon disulfide were studied in acetonitrile. Reactions orders in amine (second) and carbon disulfide (first) were determined. Rate constants were determined and it was found that they increase upon addition of pyridine and decrease with an increase in temperature, copper acetate concentration, and upon going from diethyl- to dibenzylamine. The obtained results were explained in the framework of a mechanism, according to which a charge-transfer complex of the amine yields carbon disulfide type is formed at the first stage. Then this complex reacts at the limiting stage with a second amine molecule to give dithiocarbamate ion, which forms rapidly a stable complex with copper ion.

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