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

143245-63-0

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143245-63-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 143245-63-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,2,4 and 5 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 143245-63:
(8*1)+(7*4)+(6*3)+(5*2)+(4*4)+(3*5)+(2*6)+(1*3)=110
110 % 10 = 0
So 143245-63-0 is a valid CAS Registry Number.

143245-63-0SDS

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 4-Dimethylaminomethyl-2,6-di-tert.-butyl-phenoxyl

1.2 Other means of identification

Product number -
Other names -

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:143245-63-0 SDS

143245-63-0Downstream Products

143245-63-0Relevant academic research and scientific papers

Molecular recognition: II-Discrimination of specific and non-specific intermolecular interactions by means of magnetic resonance spectroscopy

Jaeger, Martin,Schuler, Paul,Stegmann, Hartmut B.,Rockenbauer, Antal

, p. 205 - 210 (1998)

The interactions of adenine- and benzimidazole-type substrates with a model receptor (Rebek's cleft) and benzoic acid were studied by magnetic resonance spectroscopy. The spectra reveal dynamic phenomena which are analysed in terms of static, two-jump and

Synthesis and inhibitory activity of alkyl(hydroxyaryl)amines

Dyubchenko,Nikulina,Terakh,Prosenko,Grigor'ev

, p. 1149 - 1155 (2008/09/17)

The reaction of ω-(4-hydroxyaryl)haloalkanes with various nitrogen-containing agents afforded primary, secondary, and tertiary amino derivatives of 2,6-dialkylphenols. For the compounds synthesized, the reaction rate constants with peroxide radicals were

Synthesis and study of the antiradical activity of substituted hydroxybenzylamines and their hydrogen chloride salts

Dyubchenko,Nikulina,Terakh,Kandalintseva,Markov,Grigor'Ev,Prosenko

, p. 330 - 334 (2007/10/03)

Different alkylated hydroxybenzylamines and their hydrogen chloride salts were synthesized. The rate constants of their reactions with peroxide radicals k1 and the stoichiometric factors of inhibition f were measured in the initiated oxidation of cumene and methyl oleate. Copyright

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