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N,N-(2-benzylmercaptoethyl)(2-methylmercaptoethyl)amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1389375-80-7

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1389375-80-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1389375-80-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,9,3,7 and 5 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1389375-80:
(9*1)+(8*3)+(7*8)+(6*9)+(5*3)+(4*7)+(3*5)+(2*8)+(1*0)=217
217 % 10 = 7
So 1389375-80-7 is a valid CAS Registry Number.

1389375-80-7Downstream Products

1389375-80-7Relevant academic research and scientific papers

Copper(II) complexes of aliphatic tridentate amine/dithioether ligands - Synthesis and molecular structures

Blomenkemper, Marc,Schr?der, Henning,Pape, Tania,Hahn, F. Ekkehardt

, p. 143 - 147 (2012)

Three new tridentate ligands (1-3) featuring a central secondary amine linked by ethylene bridges to two thioether donor functions with S-methyl or S-benzyl substituents have been synthesized and reacted with copper(II) chloride or copper(II) nitrate. The resulting complexes of type [CuX2(L)] (L = amine-dithioether ligand) 6, 7, and 9 exhibit a square-pyramidal coordination geometry with the nitrogen and sulfur donor groups of the tridentate ligand occupying three of the basal binding sites at the metal ion. Two chloro (6 and 7) or a nitrato ligand (9) originating from the metal precursor salt complete the coordination sphere of the copper(II) ion. The apical donors are bonded with significantly longer bond distances compared to identical donors in the basal plane. The weakly bound apical chloro ligand of 6 can be abstracted with silver(I) nitrate effecting the formation of the dinuclear complex 10 featuring a nitrato ligand coordinated to two copper(II) centers in a bridging fashion. For all copper(II) complexes the observed Cu-S bond distances are very similar and not significantly influenced by alteration of the alkyl group at the thioether donor function.

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