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Phenol, 2,2'-thiobis[4-(1,1-dimethylethyl)-6-[[5-(1,1-dimethylethyl)-2-hydroxyphen yl]thio]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

56857-30-8

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56857-30-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56857-30-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,8,5 and 7 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 56857-30:
(7*5)+(6*6)+(5*8)+(4*5)+(3*7)+(2*3)+(1*0)=158
158 % 10 = 8
So 56857-30-8 is a valid CAS Registry Number.

56857-30-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[3-[3-(5-t-butyl-2-hydroxyphenylthio)-5-t-butyl-2-hydroxyphenylthio]-5-t-butyl-2-hydroxyphenylthio]-4-t-butylphenol

1.2 Other means of identification

Product number -
Other names 2-{3-[3-(5-t-butyl-2-hydroxyphenylthio)-5-t-butyl-2-hydroxyphenylthio]-5-t-butyl-2-hydroxyphenylthio}-4-t-butylphenol

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:56857-30-8 SDS

56857-30-8Relevant academic research and scientific papers

Breaking thiacalix[4]arene into pieces-a novel synthetic approach to higher calixarenes bearing mixed (-S-, -CH2-) bridges

Dvorakova, Hana,Eigner, Vaclav,Kaiser, Lukas,Landovsky, Tomas,Lhotak, Pavel,Salvadori, Karolina

, p. 36934 - 36941 (2021/12/02)

A novel approach to calix[5-7]arenes possessing mixed (S and CH2) bridges within the skeleton is based on the reaction of thiacalix[4]arene monosulfoxide with BuLi leading to a linear phenolic tetramer in essentially quantitative yield. This key intermedi

Synthesis and Inclusion Properties of Sulfur-Bridged Analogs of Acyclic Phenol-Formaldehyde Oligomers

Ohba, Yoshihiro,Moriya, Kazuhiko,Sone, Tyo

, p. 576 - 582 (2007/10/02)

A series of compounds in which a part or all of the methylene bridges of acyclic p-methyl- and p-t-butylphenol-formaldehyde tetramers were replaced by sulfur bridge(s) was synthesized.It was found that though the sulfur-bridged tetramers formed crystalline host-guest complexes with a variety of organic compounds, they were different from the parent tetramers regarding their inclusion behavior.The number and position of the sulfur bridge(s), as well as the p-substituent of phenol in the tetramers, had a great influence upon the inclusion property.The thermal stability of complexes of the sulfur-bridged tetramers (SSS-a,b) with benzene, as estimated from their thermal dissociation rates, are lower than those of the parent tetramers (CCC-a,b).

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