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Benzene, 1,1'-sulfonylbis[4-ethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

66294-51-7

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66294-51-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66294-51-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,2,9 and 4 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 66294-51:
(7*6)+(6*6)+(5*2)+(4*9)+(3*4)+(2*5)+(1*1)=147
147 % 10 = 7
So 66294-51-7 is a valid CAS Registry Number.

66294-51-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,4'-sulfonylbis(ethylbenzene)

1.2 Other means of identification

Product number -
Other names Benzene, 1,1‘-sulfonylbis[4-ethyl-

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:66294-51-7 SDS

66294-51-7Downstream Products

66294-51-7Relevant academic research and scientific papers

Facile synthesis of diarylsulfones from arenes and 3CdSO4·xH2O via mechanochemistry

Qin, Shuai,Zhang, Pu,Qin, Yu-Jun,Guo, Zhi-Xin

supporting information, (2020/01/06)

A variety of substituted diarylsulfones could be synthesized by simple arenes and 3CdSO4·xH2O in the presence of P2O5 under high-speed ball milling. It was suggest the aromatic sulfonation was performed by arene and in situ generated H2SO4, following-up by electrophilic substitution with another arene to give diarylsulfone.

The synthesis of diarylsulfones with simple arenes and K2S2O8 through double C-S bond formation

Yang, Yiqing,Chen, Zhang,Rao, Yu

supporting information, p. 15037 - 15040 (2014/12/11)

An unprecedented double C-S bond formation method has been developed to prepare both symmetric and unsymmetric diarylsulfones with simple arenes in a single step. This represents the first example that K2S2O8 can be employed as a highly effective sulfonating agent to synthesize diarylsulfones. The reaction demonstrates excellent reactivity, good functional group tolerance and high yields.

Sulfosilylation of Aromatic Hydrocarbons by Trimethylsilyl Chlorosulfonate

Hofmann, Karin,Simchen, Gerhard

, p. 282 - 297 (2007/10/02)

Aromatic hydrocarbons 2 ,6 ,8 ,9 ,13 ,16 ,18 ,19 ,22 react with trimethylsilyl chlorosulfonate (1) to give trimethylsilyl arenesulfonates 5, 7, 11, 12, 15, 23 or sulfonic acids 17, 20, 21.If trimethylsilyl sulfonates are obtained, working up of the sulfonation mixtures is possible by distillation.By hydrohalogenolysis of trimethylsilyl sulfonates 5 at 0-5 deg C anhydrous sulfonic acids 3 result.The pathways to diphenylsulfone (25a) in the reaction of benzene (2a) with 1 were investigated.In this connection we succeeded in synthesizing benzenepyrosulfonic acid (28) and trimethylsilyl benzenepyrosulfonate (29).

Novel Sulfonylation reagent: Sulfuric Acid-Hexafluoroacetic Anhydride

Tyobeka, Themba E.,Hancock, Richard A.,Weigel, Helmut

, p. 114 - 115 (2007/10/02)

A mixture of sulfuric acid and hexafluoroacetic anhydride is an efficient reagent for the sulfonylation of aromatic compounds.

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