86785-33-3 Usage
Uses
Used in Pharmaceutical Research and Drug Development:
N-(2-Methyl-4-nitrophenyl)benzenesulfonamide is used as a research compound for its potential biological activity. It is employed in the development of new drugs and therapies, particularly for its anti-inflammatory and analgesic properties.
Used in Antibiotics and Antimicrobial Agents:
As a sulfonamide derivative, N-(2-Methyl-4-nitrophenyl)benzenesulfonamide is used as an antibiotic and antimicrobial agent. It is utilized in the treatment of bacterial infections and helps in controlling the growth of harmful microorganisms.
Used in Organic Chemistry:
N-(2-Methyl-4-nitrophenyl)benzenesulfonamide is used as a reagent in organic chemistry for the synthesis of other compounds. Its unique chemical structure allows it to be a valuable component in various chemical reactions and processes.
Check Digit Verification of cas no
The CAS Registry Mumber 86785-33-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,7,8 and 5 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 86785-33:
(7*8)+(6*6)+(5*7)+(4*8)+(3*5)+(2*3)+(1*3)=183
183 % 10 = 3
So 86785-33-3 is a valid CAS Registry Number.
InChI:InChI=1/C13H12N2O4S/c1-10-9-11(15(16)17)7-8-13(10)14-20(18,19)12-5-3-2-4-6-12/h2-9,14H,1H3
86785-33-3Relevant academic research and scientific papers
USE OF DDX3 INHIBITORS AS ANTIPROLIFERATIVE AGENTS
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Page/Page column 69; 70; 71; 72, (2017/10/30)
The present invention refers to compounds of formula I or II endowed with DDX3 inhibitory activity, relative pharmaceutical compositions and their use as antihyperproliferative agents. (I) or (II)
Preparation of Nonsymmetrical p-Benzoquinone Diimines for Evaluation as Protein Cleavage Reagents
Holmes, Thomas J.,Lawton, Richard G.
, p. 3146 - 3150 (2007/10/02)
In an effort to improve the yield, selectivity, and mildness of reaction conditions employed in protein cleavage with bisalkylating quinone diimines, a series of analogous reagents (1a-h) were prepared.These novel N1,N4 nonsymmetrica
