53731-86-5 Usage
Uses
Used in Pharmaceutical Synthesis:
1-hydroxy-3-(4-methylphenyl)urea is used as an intermediate in the synthesis of pharmaceuticals for its potential role in developing antitumor and antiviral agents.
Used in Agrochemical Production:
1-hydroxy-3-(4-methylphenyl)urea is also utilized in the production of agrochemicals, contributing to the development of effective crop protection solutions.
Used in Organic Reactions:
1-hydroxy-3-(4-methylphenyl)urea serves as a reactant in various organic reactions, facilitating the creation of new chemical entities.
Used in Medicinal Chemistry Research:
It is employed as a research tool in medicinal chemistry to explore its potential applications in treating specific diseases and conditions.
Used in Cancer Treatment:
1-hydroxy-3-(4-methylphenyl)urea is studied for its potential role in inhibiting the growth of certain cancer cells, making it a candidate for further research in oncology.
Used as a Corrosion Inhibitor:
In some industrial processes, 1-hydroxy-3-(4-methylphenyl)urea has been studied for its potential as a corrosion inhibitor, offering protection to materials from degradation.
Check Digit Verification of cas no
The CAS Registry Mumber 53731-86-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,7,3 and 1 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 53731-86:
(7*5)+(6*3)+(5*7)+(4*3)+(3*1)+(2*8)+(1*6)=125
125 % 10 = 5
So 53731-86-5 is a valid CAS Registry Number.
53731-86-5Relevant academic research and scientific papers
N-substituted hydroxyureas as urease inhibitors
Uesato, Shinichi,Hashimoto, Yuichiro,Nishino, Masaru,Nagaoka, Yasuo,Kuwajima, Hiroshi
, p. 1280 - 1282 (2007/10/03)
In order to seek a urease inhibitor more potent than hydroxyurea (1), its alkyl- or phenyl-substituted derivatives were synthesized and evaluated for their effect on the jack bean urease. Of 16 compounds tested, m-methyl-(10) and m-methoxy-phenyl substituted hydroxyurea (13) showed the most potent inhibitory activities against the enzyme.
