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2-((2-((3-5-di-tert-butyl-2-hydroxybenzyl)(2-hydroxyethyl)amino)ethyl amino)methyl)-4,6-di-tert-butylphenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1290137-33-5

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1290137-33-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1290137-33-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,9,0,1,3 and 7 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1290137-33:
(9*1)+(8*2)+(7*9)+(6*0)+(5*1)+(4*3)+(3*7)+(2*3)+(1*3)=135
135 % 10 = 5
So 1290137-33-5 is a valid CAS Registry Number.

1290137-33-5Downstream Products

1290137-33-5Relevant academic research and scientific papers

Oxygenation of sulfides catalysed by SBA-15-immobilized molybdenum(VI) complex of a bis(phenol) diamine ligand using aqueous hydrogen peroxide as a green oxidant

Saberikia, Iraj,Safaei, Elham,Karimi, Babak,Lee, Yong-Iii

, (2018)

A highly efficient and reusable molybdenum-based catalyst has been synthesized by covalent grafting of a bis(phenol) diamine ligand, namely 2-(((2-bromoethyl)(2-((3,5-di-tert-butyl-2-hydroxybenzyl)amino)ethyl)amino)methyl)-4,6-di-tert-butylphenol, onto functionalized ordered mesoporous silica (SBA-15) followed by complexation with MoO2(acac)2. The resulting organic–inorganic hybrid material was found to be a highly effective catalyst for oxygenation of various sulfides to their corresponding sulfoxides or sulfones. The catalyst was characterized using transmission and scanning electron microscopies, X-ray photoelectron, Fourier transform infrared and atomic absorption spectroscopies, Brunauer–Emmett–Teller surface area analysis and thermogravimetric analysis. Mild reaction conditions, high selectivity and easy recovery and reusability of the catalyst render the presented protocol very useful for addressing industrial needs and environmental concerns.

Synthesis and characterization of two binuclear iron(III) complexes of aminoethanol derivatives of aminophenol as models for non-heme iron enzymes active sites

Safaei, Elham,Saberikia, Iraj,Wojtczak, Andrzej,Jagli?i?, Zvonko,Kozakiewicz, Anna

, p. 1143 - 1148 (2011)

Two aminoethanol derivatives of aminophenol ligands were synthesized and characterized by IR and 1H NMR spectroscopies. The binuclear iron(III) complexes of these ligands have been prepared and characterized by IR, 1H NMR and UV-Vis

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