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Phenoxy, 2,6-bis(1,1-dimethylethyl)-4-[3-(octadecyloxy)-3-oxopropyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

57559-04-3

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57559-04-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57559-04-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,5,5 and 9 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 57559-04:
(7*5)+(6*7)+(5*5)+(4*5)+(3*9)+(2*0)+(1*4)=153
153 % 10 = 3
So 57559-04-3 is a valid CAS Registry Number.

57559-04-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name n-octadecyl-3-(3,5-di-tert-butyl-4-hydroxyphenyl)-propionate radical

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:57559-04-3 SDS

57559-04-3Relevant academic research and scientific papers

Localized electron transfer in nonpoiar solution: reaction of phenols and thiophenols with free solvent radical cations

Brede, Ortwin,Ganapathi, Mahalaxmi R.,Naumov, Sergej,Naumann, Wolfgang,Hermann, Ralf

, p. 3757 - 3764 (2001)

Free electron transfer (FET) is understood as the reaction of free and uncorrelated solvent parent radical cations with solutes characterized by a lower ionization potential than those of the solvent. We studied electron transfer from phenols and thiophen

Free electron transfer from several phenols to radical cations of non-polar solvents

Ganapathi,Hermann,Naumov,Brede

, p. 4947 - 4955 (2007/10/03)

Electron-transfer reactions from phenols to parent radical cations of solvents were studied using pulse radiolysis. Phenols bearing electron-withdrawing, electron-donating and bulky substituents were investigated in non-polar solvents such as cyclohexane, n-dodecane, n-butyl chloride and 1,2-dichloroethane. The experiments revealed the direct, synchronous formation of phenoxyl radicals and phenol radical cations in all cases and in nearly the same relative amounts. This was explained by two competing electron-transfer channels which depend on the geometry of encounter between the parent solvent radical cations and the solute phenol molecules. The mechanism is analysed at a microscopic level, treating diffusion as a slow process and the local electron transfer as an extremely rapid event. Furthermore, the effect of various phenol substituents and solvent types on the electron-transfer mechanism and on the decay kinetics of the solute phenol radical cations was analysed. The results were further substantiated using a quantum chemical approach.

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