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(2,9-dimethylphenanthroline) zinc bis(benzylmercaptonate) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

216979-79-2

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216979-79-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 216979-79-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,6,9,7 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 216979-79:
(8*2)+(7*1)+(6*6)+(5*9)+(4*7)+(3*9)+(2*7)+(1*9)=182
182 % 10 = 2
So 216979-79-2 is a valid CAS Registry Number.

216979-79-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,9-dimethylphenanthroline) zinc bis(benzylmercaptonate)

1.2 Other means of identification

Product number -
Other names (2,9-dimethylphenanthroline)Zn(SCH2Ph)2

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:216979-79-2 SDS

216979-79-2Relevant academic research and scientific papers

(Neocuproin)zinc Thiolates: Attempts at Modeling Cobalamin-Independent Methionine Synthase

Seebacher, Jan,Ji, Mian,Vahrenkamp, Heinrich

, p. 409 - 417 (2007/10/03)

Several new complexes [(neo)Zn(SR)2] [neo = neocuproin (2,9-dimethylphenanthroline)] have been synthesized and structurally characterised. They react in a stepwise fashion with the alkylating agents CH3I and (CH3)2SO4 to afford the thioethers CH3SR and first the mixed complexes [(neo)Zn(SR)X] (X = I, CH3SO4) and then [(neo)ZnX2]. Similar alkylations occur with benzyl iodide, but not with trimethyl phosphate in nonpolar media. Under these conditions, thiolate exchange with [PPN]SR does not occur which indicates that the alkylations take place at the zinc-bound thiolates. In polar solvents (methanol, DMSO), thiolate exchange occurs readily, and at higher temperatures (CH3)3PO4 also acts as an alkylating agent which indicates that under these conditions free thiolate is available in solution. Qualitative kinetic data support the associative alkylation mechanism in nonpolar media and the change of mechanism in polar media. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004.

Zinc thiolate complexes with chelating nitrogen ligands

Burth,Vahrenkamp

, p. 193 - 199 (2008/10/08)

The thiolates SPh-, SCH2Ph- and SCH2CH2Ph- were combined with polydentate nitrogen donor ligands in monomeric zinc complexes. N-substituted bis(benzimidazolylmethyl)sulfides (R-BIMS) yielded the complexes (R-BIMS)Zn(SR)2 (1-3) in which the central thioether sulfur does not coordinate. This holds also for the o-hydroxymethyl-thiophenolate complex (4). 2,9-Dimethylphenanthroline (neocuproin, NEO) produced compounds (NEO)Zn(SR)2 (5). Bis(dimethylpyrazolyl-N-ethyl)amine (PEA) led to (PEA)Zn(SPh)2 (6) in which only one pyrazole nitrogen and the central amine nitrogen are coordinated. 2-Mercaptomethylpyridine (HMMP) formed the bis-ligand complex (MMP)2Zn (7). Six structure determinations have shown that all complexes are characterized by a tetrahedral ZnN2S2 coordination, irrespective of the ring size (5,6, 8) which is thereby enforced on the chelate ligand, even at the expense of unused ligand donor atoms.

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