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Phenol, 2-[[[2,6-bis(1-methylethyl)phenyl]imino]methyl]-4,6-bis(1,1-dimethylethyl) - is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

210882-24-9

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210882-24-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 210882-24-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,0,8,8 and 2 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 210882-24:
(8*2)+(7*1)+(6*0)+(5*8)+(4*8)+(3*2)+(2*2)+(1*4)=109
109 % 10 = 9
So 210882-24-9 is a valid CAS Registry Number.

210882-24-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-di-tert-butyl-6-(2,6-diisopropylphenyliminomethyl)phenol

1.2 Other means of identification

Product number -
Other names 2,4-di-tert-butyl-6-((2,6-diisopropylphenylimino)methyl)phenol

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:210882-24-9 SDS

210882-24-9Relevant academic research and scientific papers

Structural diversity and versatility for organoaluminum complexes supported by mono- and di-anionic aminophenolate bidentate ligands

Maisse-Franois, Aline,Azor, Laurine,Schmitt, Anne-Laure,Coquel, Ariane,Brelot, Lydia,Welter, Richard,Bellemin-Laponnaz, Stéphane,Dagorne, Samuel

, p. 4248 - 4256 (2012)

The present contribution describes the synthesis and structural characterization of structurally diverse organoaluminum species supported by variously substituted aminophenolate-type ligands: these Al complexes are all derived from the reaction of AlMesu

Metal and ligand-substituent effects in the immortal polymerization of rac -lactide with Li, Na, and K phenoxo-imine complexes

Garca-Valle, Francisco M.,Estivill, Robert,Gallegos, Carlos,Cuenca, Toms,Mosquera, Marta E. G.,Tabernero, Vanessa,Cano, Jess

, p. 477 - 487 (2015)

A series of lithium, sodium, and potassium complexes with phenoxo-imine ligands M[(O-2-(RN=CH)C6H4] [R = C6H5; 2-tBuC6H5; 2,6-iPr2C6H3

Unexpected Precatalyst σ-Ligand Effects in Phenoxyimine Zr-Catalyzed Ethylene/1-Octene Copolymerizations

Gao, Yanshan,Christianson, Matthew D.,Wang, Yang,Chen, Jiazhen,Marshall, Steve,Klosin, Jerzy,Lohr, Tracy L.,Marks, Tobin J.

, p. 7822 - 7830 (2019)

Recent decades have witnessed intense research efforts aimed at developing new homogeneous olefin polymerization catalysts, with a primary focus on metal-Cl or metal-hydrocarbyl precursors. Curiously, metal-NR2 precursors have received far less

Ethylene polymerization by salicylaldimine nickel(II) complexes containing a dibenzhydryl moiety

Hu, Xiaohui,Dai, Shengyu,Chen, Changle

, p. 1496 - 1503 (2016/02/03)

The synthesis, characterization and ethylene polymerization properties of a series of salicylaldimine Ni(ii) complexes with a dibenzhydryl moiety are described. These Ni complexes are designed to bear systematically varied electron donating and withdrawin

Vanadium(III) phenoxyimine complexes for ethylene or ε-caprolactone polymerization: Mononuclear versus binuclear pre-catalysts

Clowes, Lucy,Walton, Mark,Redshaw, Carl,Chao, Yimin,Walton, Alex,Elo, Pertti,Sumerin, Victor,Hughes, David L.

, p. 152 - 160 (2013/04/10)

The mononuclear {[C6H4NCH(ArO)]2VCl(THF)} (Ar = 2,4-t-Bu2C6H2 (1), Ar = C 6H4 (2)), {O[C6H4NCH(ArO)] 2}VCl(THF) (Ar = 2,4-t-Bu2C6H2 (3), Ar = C6H4 (4)) and the binuclear vanadium(iii) complexes {[C6H4NCH(ArO)]VCl2(THF)2} 2(μ-CH2CH2) (Ar = 2,4-t-Bu2C 6H2 (5), Ar = C6H4 (6)), have been synthesized and fully characterized. The compounds [C6H 5NCH(ArO)]VCl2(THF)2 (Ar = 2,4-t-Bu 2C6H2 (7), Ar = C6H4 (8)), [2,4,6-Me3-C6H2NCH(ArO)]VCl2 (Ar = 2,4-t-Bu2C6H2 (9), Ar = C 6H4 (10)) and [2,6-i-Pr2-C6H 3NCH(ArO)]VCl2(THF)2 (Ar = 2,4-t-Bu 2C6H2 (11), Ar = C6H4 (12)), {μ-CH2CH2[NCH(C6H4O)] 2VCl(THF)} (14) and {C6H4[NCH(C 6H4O)]2VCl(THF)} (15) were synthesized for comparative polymerization studies. The dizwitterionic compound [2,6-i-Pr 2-C6H3N+(H)CH(C6H 4O)]2VCl2O (13) was also isolated, and presumably formed via a fortuitous hydrolysis reaction. The complexes 2, 5 and 13 have been structurally characterized; the molecular structure of the parent ligand (L5) in 5 is also reported. All complexes have been screened for ethylene as well as ε-caprolactone polymerization, and results are compared against those for known related mono- and bi-nuclear counterparts to evaluate for possible cooperative effects. The compounds 10 and 12 have been supported on modified SiO2, analysed by XPS and subjected to homo-polymerization (ethylene) and co-polymerization (1-hexene and ethylene) studies. The Royal Society of Chemistry 2013.

The use of Cu and Zn salicylaldimine complexes as catalyst precursors in ring opening polymerization of lactides: Ligand effects on polymer characteristics

Bhunora, Suraj,Mugo, Jane,Bhaw-Luximon, Archana,Mapolie, Selwyn,Van Wyk, Juanita,Darkwa, James,Nordlander, Ebbe

experimental part, p. 133 - 145 (2012/06/18)

A range of monomeric tetra-coordinate copper (II) and zinc (II) complexes based on N,O-bidentate salicylaldimine Schiff base ligands has been synthesized and characterized using various spectroscopic techniques. These complexes were then evaluated as init

Synthesis and characterisation of neutral dialkylaluminium complexes stabilised by salicylaldiminato ligands, and their conversion to monoalkylaluminium cations

Cameron,Gibson,Redshaw,Segal,Solan,White,Williams

, p. 1472 - 1476 (2007/10/03)

Treatment of the salicylaldimine ligands 3,5-But2-2-(OH)C6 H2CHNR [R = 2,6-Me2C6H3 (1a), 2,6-Pri2C6H3 (1b), 3,5-(CF3)2

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