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N-(3-methylphenyl)-4-chlorobenzene sulfonamide is a chemical compound with the molecular formula C13H12ClNO2S. It is an organic compound that belongs to the class of sulfonamides, which are known for their antimicrobial properties. This specific compound features a 3-methylphenyl group attached to a 4-chlorobenzene sulfonamide moiety. The 3-methylphenyl group contributes to the compound's lipophilicity, while the 4-chlorobenzene sulfonamide part is responsible for its potential biological activity. Although not widely used in pharmaceuticals, N-(3-methylphenyl)-4-chlorobenzene sulfonamide serves as a structural analog to other sulfonamides that have been employed as antibacterial agents. Its chemical structure and properties make it a subject of interest in the field of organic chemistry and drug design, where it could potentially be modified to enhance its therapeutic effects or to study its interactions with biological targets.

7454-50-4

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7454-50-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7454-50-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,5 and 4 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7454-50:
(6*7)+(5*4)+(4*5)+(3*4)+(2*5)+(1*0)=104
104 % 10 = 4
So 7454-50-4 is a valid CAS Registry Number.

7454-50-4Relevant academic research and scientific papers

Synthesis of N -Arylsulfonamides by a Copper-Catalyzed Reaction of Chloramine-T and Arylboronic Acids at Room Temperature

Ouyang, Banlai,Liu, Deming,Xia, Kejian,Zheng, Yanxia,Mei, Hongxin,Qiu, Guanyinsheng

supporting information, p. 111 - 115 (2017/12/27)

A copper-catalyzed Chan-Lam-coupling-like reaction of a (het)arylboronic acid and chloramine-T (or a related compound) has been developed for the synthesis of N -arylsulfonamides at room temperature in moderate to good yields, with good tolerance of functional groups. In this process, it is believed that chloramine-T serves as an electrophile.

Copper-catalyzed cross-coupling of chloramine salts and arylboronic acids in water: A green and practical route to N-arylsulfonamides

Ouyang, Banlai,Zheng, Yanxia,Liu, Yi,Liu, Fei,Yao, Juying,Peng, Yiyuan

, p. 3694 - 3698 (2018/09/14)

A green and practical method for the synthesis of N-arylsulfonamides from chloramine salts and arylboronic acids is herein developed. The reaction proceeds readily in the presence of 5 mol% of CuI and 2.5 equiv. K2CO3 in water at room temperature, generating a variety of N-arylsulfonamides in moderate to good yields with good functional group tolerance.

Synthesis and screening of in vitro antibacterial and enzyme inhibitory activity of N,N-disubstituted 4-chlorobenzenesulfonamides

Aziz-ur-Rehman,Nafeesa, Khadija,Abbasi, Muhammad Athar,Nadeem, Sohail,Khan, Khalid Mohammed,Ahmad, Irshad,Afzal, Saira

, p. 1096 - 1104 (2015/01/30)

Sulfonamide, pharmacologically important class of compounds, is of significant interest for scientists due to increased resistance in microbes against the existing drug constituents. So the aim of following research work was to synthesize new more effecti

Synthesis, structural analysis and pharmacological screening of chlorinated sulfonamides

Aziz-Ur-Rehman,Tahir, Saif-Ur-Rehman,Abbasi, Muhammad Athar,Rasool, Shahid,Siddiqa, Asia,Awais-Ur-Rehman,Muhammad, Ali,Sharif, Ahsan

, p. 9000 - 9004 (2013/11/19)

In present work, a facile and environmentally benign series of chlorinated sulfonamides was synthesized and screened against different enzymes. These were geared up by the coupling of 4-chlorobenzenesulfonyl chloride (1) with different substituted aromatic amines (2a-l) under dynamic pH control in aqueous media to form various chlorinated sulfonamides (3a-l). The synthesized chlorinated sulfonamides were spectrally characterized like 1H NMR, IR and EI-MS. The bioactivity of all the synthesized compounds were evaluated against urease, butyrylcholinesterase (BChE) and lipoxygenase (LOX) enzymes and found to be having talented activity against butyrylcholinesterase enzyme.

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