99362-55-7 Usage
Description
(2-methoxy-benzyl)-urea is a chemical compound with the molecular formula C9H12N2O2. It is a urea derivative featuring a methoxybenzyl group attached to the urea nitrogen atom. (2-methoxy-benzyl)-urea holds potential applications in pharmaceutical and medicinal chemistry due to the known biological activities of urea derivatives. The methoxybenzyl group's steric hindrance and electronic effects may further influence the compound's reactivity and pharmacological properties, warranting further research to explore its full potential.
Uses
Used in Pharmaceutical Industry:
(2-methoxy-benzyl)-urea is used as a pharmaceutical intermediate for the synthesis of various drugs. Its unique structure allows it to serve as a building block in the development of new medicinal compounds with potential therapeutic applications.
Used in Medicinal Chemistry Research:
(2-methoxy-benzyl)-urea is utilized as a research compound in medicinal chemistry. It aids scientists in understanding the structure-activity relationships of urea-based drugs and contributes to the discovery of novel therapeutic agents.
Further research and studies are necessary to fully understand the potential uses and implications of (2-methoxy-benzyl)-urea in different fields, including its possible role in drug delivery systems or as a modulator of biological targets.
Check Digit Verification of cas no
The CAS Registry Mumber 99362-55-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,3,6 and 2 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 99362-55:
(7*9)+(6*9)+(5*3)+(4*6)+(3*2)+(2*5)+(1*5)=177
177 % 10 = 7
So 99362-55-7 is a valid CAS Registry Number.
99362-55-7Relevant articles and documents
Microwave-assisted synthesis of N-monosubstituted urea derivatives
De Luca, Lidia,Porcheddu, Andrea,Giacomelli, Giampaolo,Murgia, Irene
scheme or table, p. 2439 - 2442 (2010/11/18)
An easy and rapid procedure for the preparation of N-monosubstituted ureas via reaction between potassium cyanate and a wide range of amines is described. The procedure was performed under microwave irradiation using water as solvent. This methodology is particularly attractive since it provides ureas in high yield and purity. Georg Thieme Verlag Stuttgart · New York.
