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(4-fluoro-2-formylphenyl)phenylthioether is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1158577-41-3

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1158577-41-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1158577-41-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,5,8,5,7 and 7 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1158577-41:
(9*1)+(8*1)+(7*5)+(6*8)+(5*5)+(4*7)+(3*7)+(2*4)+(1*1)=183
183 % 10 = 3
So 1158577-41-3 is a valid CAS Registry Number.

1158577-41-3Downstream Products

1158577-41-3Relevant academic research and scientific papers

Efficient synthesis of unsymmetrical diaryl thioethers via TBAF-mediated denitrative substitution of nitroarenes with PhSTMS under mild and neutral conditions

Yu, Xiao-Chun,Li, Bo,Yu, Bao-Hua,Xu, Qing

, p. 605 - 608 (2013)

Tetrabutylammonium fluoride (TBAF) effectively facilitated a denitrative substitution reaction of electron-deficient nitroarenes with phenylthiotrimethylsilane (PhSTMS) under mild and base-free neutral conditions at room temperature, providing a practical and efficient synthesis of useful unsymmetrical diaryl thioethers. Nitroarenes bearing ortho- and para-positioned electron-withdrawing groups are the most reactive substrates, indicating that this reaction most possibly proceeded via the nucleophilic aromatic substitution (SNAr) mechanism.

TBAF-catalysed facile synthesis of unsymmetrical diaryl thioethers via mild SNAr reactions

Yu, Baohua,Zang, Xufeng,Yu, Xiaochun,Xu, Qing

, p. 351 - 353 (2010)

By using tetrabutylammonium fluoride as the catalyst, the synthesis of unsymmetrical diaryl thioethers could be easily achieved in high yields via a mild nucleopilic aromatic substitution reaction of aryl fluorides and phenylthiotrimethylsilane.

New CRTH2 Antagonists

-

Page/Page column 31-32, (2012/12/13)

The present invention relates to a compound of formula (I), to the process for preparing such compounds and to their use in the treatment of a pathological condition or disease susceptible to amelioration by CRTh2 antagonist activity.

Microwave-promoted TBAF-catalyzed SNAr reaction of aryl fluorides and ArSTMS: An efficient synthesis of unsymmetrical diaryl thioethers

Liu, Chuanzhi,Zang, Xufeng,Yu, Baohua,Yu, Xiaochun,Xu, Qing

supporting information; experimental part, p. 1143 - 1148 (2011/07/09)

Microwave irradiation was found to promote tetrabutylammonium fluoride catalyzed nucleophilic aromatic substitution of aryl fluorides and arylthiotrimethylsilanes, affording high yields of unsymmetrical diaryl thioethers efficiently under mild, transition-metal- and base-free conditions. Microwave showed unusual improvement on the reaction in not only the conditions and reaction rate, but also in selectivity and substrate scope. Georg Thieme Verlag Stuttgart - New York.

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