6297-92-3 Usage
Chemical structure
A urea derivative containing a furan ring and a nitrophenyl group.
Functional groups
Furan ring, nitrophenyl group, urea group.
Molecular weight
Approximately 238.21 g/mol.
Appearance
Likely a solid or crystalline material, though the exact appearance is not provided in the material.
Applications
Commonly used as a building block in the synthesis of various pharmaceuticals and agrochemicals.
Biological activities
Potential anti-inflammatory and analgesic properties.
Drug development
Valuable target for drug development due to its potential biological activities.
Research potential
Unique structure and potential pharmacological properties make it a promising candidate for further research in the field of medicinal chemistry.
Safety
The material does not provide information on safety, but as a chemical compound, it is important to follow proper handling and storage procedures to minimize risks.
Check Digit Verification of cas no
The CAS Registry Mumber 6297-92-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,9 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6297-92:
(6*6)+(5*2)+(4*9)+(3*7)+(2*9)+(1*2)=123
123 % 10 = 3
So 6297-92-3 is a valid CAS Registry Number.
6297-92-3Relevant 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.