19766-54-2 Usage
Uses
Used in Organic Synthesis:
N-[4-(dimethylamino)phenyl]benzenesulfonamide is used as a reagent in organic synthesis for its ability to participate in various chemical reactions, contributing to the formation of new compounds with potential applications in different industries.
Used in Pharmaceutical Research:
In pharmaceutical research, N-[4-(dimethylamino)phenyl]benzenesulfonamide is utilized as a starting material or intermediate in the development of new drugs. Its potential to inhibit certain enzymes makes it a candidate for the treatment of various diseases.
Used in Disease Treatment:
N-[4-(dimethylamino)phenyl]benzenesulfonamide is studied for its potential use in the treatment of diseases such as cancer and microbial infections. Its ability to target specific enzymes and pathways involved in these diseases offers a promising avenue for therapeutic intervention.
Used in Anti-inflammatory and Antioxidant Applications:
The anti-inflammatory and antioxidant properties of N-[4-(dimethylamino)phenyl]benzenesulfonamide are being investigated for their potential to alleviate inflammation and protect against oxidative stress, which are common in various pathological conditions.
It is important to handle and dispose of N-[4-(dimethylamino)phenyl]benzenesulfonamide in accordance with proper safety and environmental standards due to its chemical nature.
Check Digit Verification of cas no
The CAS Registry Mumber 19766-54-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,7,6 and 6 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 19766-54:
(7*1)+(6*9)+(5*7)+(4*6)+(3*6)+(2*5)+(1*4)=152
152 % 10 = 2
So 19766-54-2 is a valid CAS Registry Number.
19766-54-2Relevant academic research and scientific papers
Khazalpour, Sadegh,Nematollahi, Davood,Ahmad, Azizan,Dowlati, Bahram
, p. 909 - 913 (2015)
To the best of our knowledge, this is first report describing generation of Michael acceptor via electrochemical reduction. In this work, electrochemical reduction of 4-nitroso-N,N-dimethylaniline has been studied in the presence of arylsulfinic acids in
Sequential C-S and S-N Coupling Approach to Sulfonamides
Chen, Kai,Chen, Wei,Han, Bing,Chen, Wanzhi,Liu, Miaochang,Wu, Huayue
supporting information, p. 1841 - 1845 (2020/03/04)
A one-pot three-component reaction involving nitroarenes, (hetero)arylboronic acids, and potassium pyrosulfite leading to sulfonamides was described. A broad range of sulfonamides bearing different reactive functional groups were obtained in good to excellent yields through sequential C-S and S-N coupling that does not require metal catalysts.
Chemical and electrochemical oxidative coupling of N,N-dialkyl-p- phenylenediamines and arylsulfinic acids. Synthesis of sulfonamide derivatives
Nematollahi,Mehdipour,Zeinodini-Meimand,Maleki
experimental part, p. 6447 - 6450 (2010/12/30)
Electrochemical and chemical oxidation of N,N-dialkyl-p-phenylenediamines have been studied in the presence of arylsulfinic acids as nucleophiles in aqueous solutions for the synthesis of sulfonamide derivatives. The results indicate that the electrochemi
