50717-64-1 Usage
Uses
Used in Pharmaceutical Applications:
1-(2-aminophenyl)-3-(2-methylphenyl)thiourea is utilized as a pharmaceutical agent for its anti-cancer properties. It has demonstrated potential in targeting various types of cancer cells, making it a valuable compound in the ongoing search for effective cancer treatments.
Used in Anti-Inflammatory Applications:
In addition to its anti-cancer capabilities, 1-(2-aminophenyl)-3-(2-methylphenyl)thiourea also serves as an anti-inflammatory agent. It may be used to alleviate inflammation and associated symptoms, contributing to the development of novel treatments for inflammatory conditions.
Used in Scientific Research:
1-(2-aminophenyl)-3-(2-methylphenyl)thiourea is employed as a chemical reagent in scientific research. Its unique structure and reactivity make it a valuable tool for various experimental purposes, including the investigation of biological processes and the development of new methodologies in chemical and medicinal research.
Used in Drug Development and Medicinal Chemistry Studies:
1-(2-aminophenyl)-3-(2-methylphenyl)thiourea's structure and reactivity also make it a potential candidate for further drug development and medicinal chemistry studies. Researchers may use 1-(2-aminophenyl)-3-(2-methylphenyl)thiourea as a starting point for designing new drugs or modifying existing ones to improve their efficacy and safety profiles.
Check Digit Verification of cas no
The CAS Registry Mumber 50717-64-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,7,1 and 7 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 50717-64:
(7*5)+(6*0)+(5*7)+(4*1)+(3*7)+(2*6)+(1*4)=111
111 % 10 = 1
So 50717-64-1 is a valid CAS Registry Number.
50717-64-1Relevant articles and documents
Potassium Periodate Mediated Oxidative Cyclodesulfurization toward Benzofused Nitrogen Heterocycles
Duangkamol, Chuthamat,Pattarawarapan, Mookda,Phakhodee, Wong
, p. 1981 - 1990 (2020/07/03)
A convenient oxidative cyclodesulfurization method toward the synthesis of benzofused nitrogen heterocycles using inexpensive and readily available potassium periodate as an oxidant was developed. Upon treating isothiocyanates with ortho -substituted anilines bearing N, N -, N, O -, and N, S -bis-nucleophiles, followed by an intramolecular cyclization of the in situ generated monothioureas, substituted 2-aminobenzazole series were rapidly accessible in good to excellent yields. The protocol can accommodate various substituents on both substrates while allowing more efficient, greener, and operational simpler process relative to other oxidative coupling reactions. Tetracyclic quinazolinone derivatives were also afforded in high yields in a single preparative step and chromatography-free.
Synthesis of novel benzo-1,2,5-thiadiazines, their antimicrobial activity and isomerization into benzo-1,2,4-triazines
Deohate, Pradip P.,Deohate, Jyoti P.,Berad
, p. 775 - 777 (2007/10/03)
Benzo[c]-6-aryl/alkylimino-1,2,5-thiadiazines (4a-g) have been obtained by the basification of benzo[c]-6-aryl/alkylimino-1,2,5-thiadiazine dihydroiodides (3a-g). The latter were synthesized by the oxidative cyclisation of substituted 1-aryl/alkyl-3-(2′-a
