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N-(4-chloro-benzenesulfonyl)-N'-(3,4-dichloro-phenyl)-urea is a chemical compound with the molecular formula C13H8Cl3N2O2S. It is a derivative of urea, featuring a sulfonyl group attached to a 4-chlorobenzene ring and a 3,4-dichlorophenyl group connected to the urea moiety. N-(4-chloro-benzenesulfonyl)-N'-(3,4-dichloro-phenyl)-urea is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as a building block for the development of herbicides and other bioactive molecules. Its structure provides a foundation for further chemical modifications, allowing for the exploration of its properties and potential uses in chemical research and development.

96460-34-3

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96460-34-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96460-34-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,4,6 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 96460-34:
(7*9)+(6*6)+(5*4)+(4*6)+(3*0)+(2*3)+(1*4)=153
153 % 10 = 3
So 96460-34-3 is a valid CAS Registry Number.

96460-34-3Downstream Products

96460-34-3Relevant academic research and scientific papers

Novel agents effective against solid tumors: The diarylsulfonylureas. Synthesis, activities, and analysis of quantitative structure-activity relationships

Howbert,Grossman,Crowell,Rieder,Harper,Kramer,Tao,Aikins,Poore,Rinzel,Grindey,Shaw,Todd

, p. 2393 - 2407 (2007/10/02)

A series of diarylsulfonylureas with exceptionally broad-spectrum activity against syngeneic rodent solid tumors in vivo is described. Their discovery resulted from a program dedicated to in vivo screening for novel oncolytics in solid tumor models, rather than traditional ascites leukemia models. The structures, oral efficacy, side-effect profile, and mechanism of action of these sulfonylureas appear to be distinct from previously known classes of oncolytics. An extensive series of analogues was prepared to probe structure-activity relationships (SAR), with particular focus on the substituent patterns of each aryl domain. Quantitative analysis of these substituent SARs, using the method of cluster significance analysis, showed the lipophilicity of the substituents to be the dominant determinant of activity. One compound from the series, LY186641 (104, sulofenur), has progressed to Phase I clinical trials as an antitumor drug.

N([(4-trifluoromethylphenyl)amino]carbonyl)benzene sulfonamides

-

, (2008/06/13)

This invention provides the use of certain benzenesulfonamide derivatives in the treatment of susceptible neoplasms in mammals. Also provided are certain novel benzenesulfonamide derivatives and their pharmaceutical formulations.

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