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Benzenesulfonamide, 4-chloro-N-(2-chloroethyl)-, also known as 4-chloro-N-(2-chloroethyl)benzenesulfonamide, is an organic compound with the chemical formula C8H8Cl2NO2S. It is a derivative of benzenesulfonamide, featuring a 4-chloro substituent and a 2-chloroethyl group attached to the nitrogen atom. Benzenesulfonamide, 4-chloro-N-(2-chloroethyl)- is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of herbicides and other chemical products. Due to its potential applications in the chemical industry, it is essential to understand its properties, reactivity, and safety considerations.

4875-54-1

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4875-54-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4875-54-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,7 and 5 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4875-54:
(6*4)+(5*8)+(4*7)+(3*5)+(2*5)+(1*4)=121
121 % 10 = 1
So 4875-54-1 is a valid CAS Registry Number.

4875-54-1Relevant academic research and scientific papers

INDOLE DERIVATIVES AND USES THEREOF FOR TREATING A CANCER

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Page/Page column 71-72; 79; 88-89, (2022/02/06)

The present invention relates to indole derivatives of formula (I') as CK2 inhibitor and pharmaceutical compositions comprising the same. The present invention further relates to the use of such compounds of formula (I) for use for preventing and/or treating a cancer.

Synthesis and bioevaluation of new 5-benzylidenethiazolidine-2,4-diones bearing benzenesulfonamide moiety

Thuan, Nguyen Thi,Dung, Do Thi Mai,Que, Do Nguyet,Dung, Phan Thi Phuong,Vu, Tran Khac,Hahn, Hyunggu,Han, Byung Woo,Kim, Youngsoo,Han, Sang-Bae,Nam, Nguyen-Hai

, p. 3803 - 3812 (2015/10/06)

Two series of new 5-benzylidenethiazolidine-2,4-diones bearing benzenesulfonamide moiety were designed and synthesized. The synthesized compounds were evaluated for several biological activities, including cytotoxicity, histone deacetylation, and protein

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