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3-methyl-4-(phenylsulfonyl)aniline is an organic compound with the molecular formula C13H13NO2S. It is a derivative of aniline, featuring a methyl group at the 3rd carbon and a phenylsulfonyl group at the 4th carbon. 3-methyl-4-(phenylsulfonyl)aniline is characterized by its aromatic structure, with the phenyl ring and the aniline group connected through a sulfonyl bridge. It is a white to off-white crystalline solid and is soluble in organic solvents. 3-methyl-4-(phenylsulfonyl)aniline is used in the synthesis of various pharmaceuticals and agrochemicals due to its unique chemical properties and reactivity. It is also employed as an intermediate in the production of dyes and pigments, as well as in the preparation of certain polymers. The compound's specific structure and reactivity make it a valuable building block in the chemical industry.

7018-99-7

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7018-99-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7018-99-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,1 and 8 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7018-99:
(6*7)+(5*0)+(4*1)+(3*8)+(2*9)+(1*9)=97
97 % 10 = 7
So 7018-99-7 is a valid CAS Registry Number.

7018-99-7Relevant academic research and scientific papers

Selective Synthesis of ortho-Substituted Diarylsulfones by Using NHC-Au Catalysts under Mild Conditions

Zhu, Haibo,Shen, Yajing,Wen, Daheng,Le, Zhang-Gao,Tu, Tao

, p. 974 - 979 (2019/02/14)

A single-step gold(I)-catalyzed chemoselective protocol to access ortho-substituted diarylsulfones has been established. Acenaphthoimidazolylidene gold complexes are effective catalysts for the arylsulfonylation of boronic acids by potassium metabisulfite (K2S2O5) and diaryliodonium salts to access (poly-)ortho-substituted diarylsulfones even in gram scale. Unlike the transition metal-catalyzed two-component coupling systems, the sterically hindered aryl groups in diaryliodonium salts are preferentially transferred over less bulky ones to form synthetically difficult targets, including those of pharmaceutical importance.

N-aryl-3,3,3-trifluoro-2-hydroxy-2-methylpropanamides: K(ATP) potassium channel openers. Modifications on the western region

Ohnmacht, Cyrus J.,Russell, Keith,Empfield, James R.,Frank, Cathy A.,Gibson, Keith H.,Mayhugh, Daniel R.,McLaren, Frances M.,Shapiro, Howard S.,Brown, Frederick J.,Trainor, Diane A.,Ceccarelli, Christopher,Lin, Margaret M.,Masek, Brian B.,Forst, Janet M.,Harris, Robert J.,Hulsizer, James M.,Lewis, Joseph J.,Silverman, Stuart M.,Smith, Reed W.,Warwick, Paul J.,Kau, Sen T.,Chun, Alexa L.,Grant, Thomas L.,Howe, Burton B.,Li, Jack H.,Trivedi, Shephali,Halterman, Tracy J.,Yochim, Christopher,Dyroff, Martin C.,Kirkland,Neilson, Kathleen L.

, p. 4592 - 4601 (2007/10/03)

A subset of antiandrogen compounds, the N-aryl-3,3,3-trifluoro-2- hydroxy-2-methylpropanamides 1, were found to activate ATP sensitive potassium channels (K(ATP)) and represent a new class of potassium channel openers (PCOs). A structure-activity relation

Therapeutic amides

-

, (2008/06/13)

Amides having formula I: STR1 wherein E, X, R2 and R3 have the meanings given in the specification, and pharmaceutically acceptable salts and pharmaceutically acceptable in vivo hydrolysable esters thereof, which are useful in the treatment of urinary incontinence. Further provided are processes for preparing the amides and pharmaceutical compositions containing them.

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