4974-07-6 Usage
General Description
1-(3-Hydroxypropyl)-3-phenylurea is a chemical compound made up of a 3-phenylurea core with a hydroxypropyl group attached to it. It is often used as a building block in the synthesis of various pharmaceuticals and agrochemicals. 1-(3-Hydroxypropyl)-3-phenylurea has potential applications in the field of medicine and agriculture due to its versatile chemical structure and reactivity. It may be utilized as a precursor in the development of new drugs or as a component in the formulation of pesticides. Additionally, it could serve as a starting material for the production of other derivatives with distinct properties and functions for use in a wide range of industries. Overall, 1-(3-Hydroxypropyl)-3-phenylurea is a valuable chemical with diverse potential applications in the field of science and technology.
Check Digit Verification of cas no
The CAS Registry Mumber 4974-07-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,7 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4974-07:
(6*4)+(5*9)+(4*7)+(3*4)+(2*0)+(1*7)=116
116 % 10 = 6
So 4974-07-6 is a valid CAS Registry Number.
4974-07-6Relevant articles and documents
A facile synthesis of unsymmetrical ureas
Bogolubsky, Andrey V.,Ryabukhin, Sergey V.,Pipko, Sergey E.,Lukin, Oleg,Shivanyuk, Alexander,Mykytenko, Dmytro,Tolmachev, Andrey
, p. 3619 - 3623 (2011/06/21)
A facile and versatile method for the synthesis of unsymmetrical ureas from readily available reagents is reported. In the first step trifluoroethylchloroformate is reacted with a stoichiometric amount of a primary amine to give an intermediate trifluoroethyl carbamate. The addition of a second amine (primary or secondary) to the trifluoroethyl carbamate furnishes corresponding unsymmetrical ureas in 75-85% yield. A simple workup procedure, the high yields obtained, and the purity of the isolated products are suitable for the parallel synthesis of combinatorial libraries of unsymmetrical ureas with high structural and functional diversity.
