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4-Chlor-benzolsulfonsaeure-<2,4-dimethyl-anilid>, also known as 4-chlorobenzenesulfonic acid 2,4-dimethylanilide, is a chemical compound with the molecular formula C14H16ClNO3S. It is a derivative of benzenesulfonic acid, where a 4-chlorophenyl group is attached to the sulfonic acid moiety, and a 2,4-dimethylaniline group is connected to the benzene ring. 4-Chlor-benzolsulfonsaeure-<2,4-dimethyl-anilid> is characterized by its white crystalline appearance and is used in various chemical reactions and industrial processes, such as the synthesis of dyes and pharmaceuticals. Due to its complex structure, it is important to handle 4-Chlor-benzolsulfonsaeure-<2,4-dimethyl-anilid> with care, following proper safety protocols to minimize potential health and environmental risks.

7454-66-2

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7454-66-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7454-66-2 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, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7454-66:
(6*7)+(5*4)+(4*5)+(3*4)+(2*6)+(1*6)=112
112 % 10 = 2
So 7454-66-2 is a valid CAS Registry Number.

7454-66-2Downstream Products

7454-66-2Relevant academic research and scientific papers

Synthesis, antibacterial and lipoxygenase activities of N-[(dimethyl substituted)phenyl]-N-(4-chlorophenyl)-4-chlorobenzenesulfonamides

Aziz-Ur-Rehman,Ahmad, Imran,Abbasi, M. Athar,Nafeesa, Khadija,Siddiqui, Sabahat Z.,Hussain, Ghulam,Rahman, Jameel,Ahmed, Irshad,Afzal, Saira

, p. 1647 - 1650 (2015)

In present research work, a new series of N-[(dimethyl substituted)phenyl]-N-(4-chlorophenyl)-4-chlorobenzenesulfonamides (5a-f) was synthesized and also evaluated for their biological activities. The reaction of 4-chlorobenzenesulfonyl chloride (1) with dimethyl substituted aniline (2a-f) in aqueous alkaline medium yielded N-[(dimethyl substituted)phenyl]-4-chlorobenzenesulfonamides (3a-f). The target compounds 5a-f were synthesized by reacting the compounds 3a-f with electrophile, 4-chlorobenzyl chloride (4) in aprotic solvent, DMF and NaH. All the synthesized compounds were characterized by IR, 1H NMR and EIMS. All the synthesized derivatives were screened for antibacterial potential and were also subjected for lipoxygenase enzyme inhibition activity.

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