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2,2′-((3,5-di-tert-butyl-2-hydroxybenzyl)azanediyl)bis(ethan-1-ol) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

209681-65-2

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209681-65-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 209681-65-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,9,6,8 and 1 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 209681-65:
(8*2)+(7*0)+(6*9)+(5*6)+(4*8)+(3*1)+(2*6)+(1*5)=152
152 % 10 = 2
So 209681-65-2 is a valid CAS Registry Number.

209681-65-2Downstream Products

209681-65-2Relevant academic research and scientific papers

Complexes of cis-dioxomolybdenum(VI) with unsymmetrical tripodal NO3-donor ligands: Synthesis, characterization and catalytic applications

Kurapati, Sathish Kumar,Maloth, Swamy,Pal, Samudranil

, p. 66 - 73 (2015)

A series of cis-dioxomolybdenum(VI) complexes of general formula cis-[MoO2(HLn)] (1-4) have been synthesized in 80-85% yields by reacting equimolar amounts of [MoO2(acac)2] (acac- = acetylacetonate) with 2,2′-(2-hydroxy-3,5-R1,R2-benzylazanediyl)diethanols (H3Ln, n = 1-4) in methanol. Characterization of the complexes has been performed by elemental analysis, spectroscopic (IR, UV-Vis, 1H and 13C NMR) and electrochemical measurements. The molecular structures of all four complexes have been determined by single-crystal X-ray diffraction studies. In each of these analogous complexes, the metal centre is in a distorted octahedral NO5 coordination sphere assembled by the single edge shared 5,5,6-membered chelate rings forming NO3-donor (HLn)2- and two cis oriented oxo groups. Crystal structures of the complexes reveal formation of discrete centrosymmetric dimeric species via a pair of reciprocal intermolecular O-HO hydrogen bonding interactions. Spectroscopic data of all the complexes are consistent with their molecular structures. In the cyclic voltammograms, the redox-active complexes display a quasi-reversible to irreversible metal centred reduction with the cathodic peak potential in the range -0.92 to -1.12 V (versus Ag/AgCl). All the complexes have been evaluated for their catalytic activities in oxidative bromination reactions of styrene and salicylaldehyde and in benzoin oxidation reaction.

Mixed-valent polynuclear cobalt complexes incorporating tetradentate phenoxyamine ligands

Ang, Joo Chuan,Mulyana, Yanyan,Ritchie, Chris,Clrac, Rodolphe,Boskovic, Colette

, p. 1124 - 1129 (2009)

The new potentially tetradentate ligand precursor 2-[(bis(2-hydroxyethyl) amino)methyl]-4,6-bis-tert-butylphenol (H3L) has been synthesized and characterized. The reaction of H3L with cobalt(ii) acetate has afforded the novel mixed-v

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