4974-07-6 Usage
Chemical Structure
1-(3-Hydroxypropyl)-3-phenylurea is composed of a 3-phenylurea core with a hydroxypropyl group attached to it.
Composition
It is made up of carbon, hydrogen, nitrogen, and oxygen atoms.
Molecular Weight
The molecular weight of 1-(3-Hydroxypropyl)-3-phenylurea is approximately 202.23 g/mol.
Appearance
It is typically a white or off-white crystalline solid.
Solubility
1-(3-Hydroxypropyl)-3-phenylurea is soluble in polar solvents such as water, methanol, and ethanol.
Reactivity
Due to its versatile chemical structure, it can undergo various chemical reactions, making it a valuable building block in the synthesis of pharmaceuticals and agrochemicals.
Applications
It has potential applications in the fields of medicine and agriculture, including the development of new drugs, formulation of pesticides, and production of other derivatives with distinct properties and functions.
Precautions
As with any chemical compound, proper handling, storage, and disposal procedures should be followed to ensure safety and minimize environmental impact.
Regulatory Status
Depending on the intended use and location, 1-(3-Hydroxypropyl)-3-phenylurea may be subject to specific regulatory requirements and guidelines.
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.
