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1-(2-hydroxyethyl)-1-methyl-3-phenylurea, a urea derivative with the molecular formula C10H14N2O2, is a chemical compound that features a phenyl group and both hydroxyethyl and methyl substituents. It is known for its potential applications in the pharmaceutical industry, organic synthesis, and medicinal chemistry, with possible biological activities that warrant investigation for its use as a drug candidate.

36097-31-1

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36097-31-1 Usage

Uses

Used in Pharmaceutical Industry:
1-(2-hydroxyethyl)-1-methyl-3-phenylurea is used as an intermediate in the synthesis of various drugs, contributing to the development of new pharmaceuticals due to its unique chemical structure and properties.
Used in Organic Synthesis:
In the field of organic synthesis, 1-(2-hydroxyethyl)-1-methyl-3-phenylurea serves as a valuable building block for creating more complex molecules, potentially leading to novel compounds with specific applications.
Used in Medicinal Chemistry:
1-(2-hydroxyethyl)-1-methyl-3-phenylurea is used as a starting material or a component in the design and synthesis of new medicinal compounds, potentially leading to the discovery of new drugs with improved efficacy and safety profiles.
Used in Drug Discovery:
Due to its potential biological activities, 1-(2-hydroxyethyl)-1-methyl-3-phenylurea may be investigated for its potential as a drug candidate, particularly in the areas of pharmaceuticals and medicinal chemistry where its unique properties could be harnessed for therapeutic purposes.

Check Digit Verification of cas no

The CAS Registry Mumber 36097-31-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,0,9 and 7 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 36097-31:
(7*3)+(6*6)+(5*0)+(4*9)+(3*7)+(2*3)+(1*1)=121
121 % 10 = 1
So 36097-31-1 is a valid CAS Registry Number.

36097-31-1Relevant academic research and scientific papers

Investigation of the Mitsunobu reaction of N-(2-hydroxyethyl)-N'- phenyl-ureas

Kim, Taek Hyeon,Lee, Gue-Jae,Cha, Mi-Hyun

, p. 2753 - 2758 (2007/10/03)

The Mitsunobu reaction of N-(2-hydroxyethyl)-ureas 1 using PPh3 and EtO2CN=NCO2Et led to the mixture of N- and O-alkylation products or a single isomer depending on the substrates.

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