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N-[(4-methylphenyl)sulfonyl]butanamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

58821-26-4

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58821-26-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58821-26-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,8,2 and 1 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 58821-26:
(7*5)+(6*8)+(5*8)+(4*2)+(3*1)+(2*2)+(1*6)=144
144 % 10 = 4
So 58821-26-4 is a valid CAS Registry Number.

58821-26-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-methylphenyl)sulfonylbutanamide

1.2 Other means of identification

Product number -
Other names butyryl-(toluene-4-sulfonyl)-amine

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:58821-26-4 SDS

58821-26-4Downstream Products

58821-26-4Relevant academic research and scientific papers

Regioselective ortho olefination of aryl sulfonamide via rhodium-catalyzed direct C-H bond activation

Xie, Weijia,Yang, Jie,Wang, Baiquan,Li, Bin

, p. 8278 - 8287 (2015/03/18)

Rh(III)-catalyzed ortho C-H olefination of aryl sulfonamide directed by the SO2NHAc group is reported. This oxidative coupling process is achieved highly efficiently and selectively with a broad substrate scope. The reactions of N-tosylacetamid

Iron-catalyzed nitrene insertion reaction for facile construction of amide compounds

Chen, Guo-Qiang,Xu, Zhen-Jiang,Liu, Yungen,Zhou, Cong-Ying,Che, Chi-Ming

scheme or table, p. 1174 - 1178 (2011/06/24)

A facile method for the construction of amide compounds from aldehydes by an iron-catalyzed nitrene insertion reaction has been developed. Both aryl and aliphatic aldehydes can directly afford the corresponding amides with an iron(II)-terpyridine (tpy) complex formed in situ as catalyst, and PhI=NTs as nitrogen source under mild reaction conditions. An ESI-MS study revealed the formation of [Fe(tpy)NTs)]+ as a reaction intermediate. Georg Thieme Verlag Stuttgart - New York.

Synthesis, characterization, and antimicrobial evaluation of sulfonamides containing N-acyl moieties catalyzed by bismuth(III) salts under both solvent and solvent-free conditions

Adibi, Hadi,Massah, Ahmad Reza,Majnooni, Mohammad Bagher,Shahidi, Sherita,Afshar, Maryam,Abiri, Ramin,Naghash, Hamid Javaherian

experimental part, p. 2753 - 2766 (2010/10/21)

Efficient N-acylation of sulfonamides with both readily available carboxylic acid chlorides and anhydrides has been carried out with catalysis by bismuth(III) salts including BiCl3 and Bi (OTf)3. The reactions proceed rapidly in both heterogeneous and solvent-free conditions and afforded the corresponding N-acylsulfonamides in good to excellent yields. The mild reaction conditions and low toxicity of bismuth salts make this procedure attractive and in close agreement with the goals of green chemistry. Some of the synthesized compounds were evaluated in vitro as antimicrobial agents against representative strains of Gram-positive (Staphylococcus aureus ATCC 25922, clinical strains of Staphylococcus aureus VISA and Enterococcus spp.) and Gram-negative bacteria (Pseudomonas aeruginosa ATCC 27853, clinical strains of Klebsiella pneumonia and Escherichia coli) and as antifungal agents against Candida albicans (clinically isolated) by both disc diffusion and minimal inhibition concentration (MIC) methods. All these bacteria and fungi studied were screened against some antibiotics to compare with our chemicals' zone diameters.

Highly efficient iron(II) chloride/N-bromosuccinimide-mediated synthesis of imides and acylsulfonamides

Wang, Feng,Liu, Hongxia,Fu, Hua,Jiang, Yuyang,Zhao, Yufen

supporting information; experimental part, p. 246 - 252 (2009/09/05)

We have developed a general and highly efficient iron(II) chloride/N-bromosuccinimide (NBS)-mediated method for the synthesis of imides and acylsulfonamides via couplings of thioesters with carboxamides/sulfonamides, and the method is simple, economical and shows practical advantages.

Facile synthesis of N-acylsulfonamide in the presence of silica chloride (SiO2-Cl) both under heterogeneous and solvent-free conditions

Massah, Ahmad Reza,Momeni, Ahmad Reza,Dabagh, Mina,Aliyan, Hamid,Naghash, Hamid Javaherian

, p. 265 - 273 (2008/03/17)

Sulfonamides were converted to the corresponding N-acyl sulfonamides with carboxylic acid chlorides and anhydrides in the presence of silica chloride. All reactions were performed in both heterogeneous and solvent-free conditions. This method provides the N-acyl sulfonamides products in good to high yield and purity. Copyright Taylor & Francis Group, LLC.

Synthesis, in vitro antibacterial and carbonic anhydrase II inhibitory activities of N-acylsulfonamides using silica sulfuric acid as an efficient catalyst under both solvent-free and heterogeneous conditions

Massah, Ahmad Reza,Adibi, Hadi,Khodarahmi, Reza,Abiri, Ramin,Majnooni, Mohammad Bagher,Shahidi, Sherita,Asadi, Beheshteh,Mehrabi, Masomeh,Zolfigol, Mohammad Ali

, p. 5465 - 5472 (2008/12/20)

Silica sulfuric acid catalyzes efficiently the reaction of sulfonamides with both carboxylic acid anhydrides and chlorides under solvent-free and heterogeneous conditions. All the reactions were done at room temperature and the N-acylsulfonamides were obtained with high yields and purity via an easy work-up procedure. This method is attractive and is in a close agreement with green chemistry. These compounds were also investigated for antibacterial activity, including Gram-positive cocci and Gram-negative bacilli, and carbonic anhydrase II inhibitory activity.

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