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N-methyl-N-[4-(methylsulfanyl)phenyl]acetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51657-90-0

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51657-90-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51657-90-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,6,5 and 7 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 51657-90:
(7*5)+(6*1)+(5*6)+(4*5)+(3*7)+(2*9)+(1*0)=130
130 % 10 = 0
So 51657-90-0 is a valid CAS Registry Number.

51657-90-0Relevant academic research and scientific papers

B2cat2-Mediated Reduction of Sulfoxides to Sulfides

Takahashi, Fumiya,Nogi, Keisuke,Yorimitsu, Hideki

supporting information, p. 3009 - 3012 (2020/03/25)

An efficient and operationally simple method for the reduction of sulfoxides to sulfides has been developed using bis(catecholato)diboron (B2cat2) as a reducing agent. The present method accommodates various functional groups which are generally prone to reduction: halides, alkynes, carbonyls, nitriles, and heterocycles are totally intact, and only sulfoxide moieties undergo reduction chemoselectively. Moreover, the remaining diboron and the resulting boron-containing wastes are readily removable, the practicality of this protocol being thus demonstrated.

Rhodium-Catalyzed ipso-Borylation of Alkylthioarenes via C-S Bond Cleavage

Uetake, Yuta,Niwa, Takashi,Hosoya, Takamitsu

supporting information, p. 2758 - 2761 (2016/06/15)

Rhodium-catalyzed transformation of alkyl aryl sulfides into arylboronic acid pinacol esters via C-S bond cleavage is reported. In combination with transition-metal-catalyzed sulfanyl group-guided regioselective C-H borylation reactions of alkylthioarenes, this method allows the synthesis of a diverse range of multisubstituted arenes.

Meta Functionalization of Anilines and Phenol

Fukui, Mineo,Ikeda, Toshiya,Oishi, Takeshi

, p. 466 - 475 (2007/10/02)

Base-promoted proton abstraction from ?-(N-tert-butyldimethylsilyl-N-methylaniline)chromium tricarbonyl (3) took place predominantly at the meta position and variously meta-substituted N-methylacetanilides 4 were obtained after reactions with electrophiles followed by oxidative decomplexation and N-acetylation.Application of the present method to variously N,N-disubstituted anilines 5 and phenols 7 was then examined and the corresponding meta substituted anilines 6 and phenol 9 were obtained.Keywords - metalation of aromatic ring; chromium tricarbonyl complex; tert-butyl dimethylsilyl protecting group; meta-substituted anilines; meta-substituted phenol; electrophilic substitution

META FUNCTIONALIZATION OF ANILINES AND PHENOL

Fukui, Mineo,Ikeda, Toshiya,Oishi, Takeshi

, p. 1605 - 1608 (2007/10/02)

Regioselective introduction of various functional groups on the meta-position of anilines and phenol was achieved by proton abstraction from chromium tricarbonyl complexes 3,5,7 with n-BuLi, followed by the addition of electrophiles and decomplexation.

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