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N-(5-chloro-2-methoxyphenyl)-2-hydroxy-3,5-dichlorobenzenesulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

943333-85-5

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943333-85-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 943333-85-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,3,3,3 and 3 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 943333-85:
(8*9)+(7*4)+(6*3)+(5*3)+(4*3)+(3*3)+(2*8)+(1*5)=175
175 % 10 = 5
So 943333-85-5 is a valid CAS Registry Number.

943333-85-5Downstream Products

943333-85-5Relevant academic research and scientific papers

Synthesis, characterization and antibacterial activity of halogenated aryl sulfonamides derived from 2-amino-4-chloroanisole

Rehman, Aziz Ur,Rasool, Shahid,Abbasi, Muhammad Athar,Nafeesa, Khadija,Fatima, Ambreen,Gul, Samreen,Hussain, Ghulam,Khan, Khalid Mohammed,Ahmad, Irshad,Afzal, Saira

, p. 446 - 452 (2014/08/05)

In the current work, a number of new N-(5-chloro-2-methoxyphenyl)aryl sulfonamides (3a-e) and N-ethyl/benzyl-N-(5-chloro-2-methoxyphenyl)aryl sulfonamides (6a-e and 7a-e) were synthesized and evaluated for their biological activities. The synthesis was carried out by coupling 2-amino-4-chloroanisole (1) with different aryl sulfonyl chlorides, 2a-e, under dynamic pH control in aqueous medium to form aryl sulfonamides, 3a-e. Further, N-ethyl/benzyl-N-(5- chloro-2-methoxyphenyl)aryl sulfonamides (6a-e and 7a-e) were synthesized by stirring 3a-e with the electrophiles, 4 and 5, in the presence of sodium hydride and N,N-dimethylformamide. The structures of the synthesized compounds were characterized from their spectral data. In addition, the in vitro antibacterial activity of all the target compounds was investigated against Gram-negative and Gram-positive bacteria using ciprofloxacin as a reference drug. Many of these compounds exhibited moderate to good activity and subtle structural changes in the substituents altered the inhibitory properties significantly.

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