61416-47-5 Usage
Derivative of oxazolone
2(3H)-Oxazolone, 3-methyl-5-phenylis a derivative of oxazolone, which is a five-membered heterocyclic compound containing one oxygen and one nitrogen atom.
Methyl and phenyl groups
This particular compound contains a methyl group (-CH3) and a phenyl group (-C6H5), which are organic functional groups that provide specific chemical and physical properties.
Reagent in organic synthesis
2(3H)-Oxazolone, 3-methyl-5-phenylis commonly used as a reagent in organic synthesis, meaning it is used in chemical reactions to produce other compounds.
Medicinal chemistry and pharmaceutical research
2(3H)-Oxazolone, 3-methyl-5-phenyl- has been studied for its potential biological activities and therapeutic applications, making it of interest in the field of medicinal chemistry and pharmaceutical research.
Ligand in coordination chemistry
2(3H)-Oxazolone, 3-methyl-5-phenylhas been investigated for its ability to function as a ligand in coordination chemistry, which involves the bonding of metal ions to organic molecules.
Building block for complex organic molecules
2(3H)-Oxazolone, 3-methyl-5-phenyl- has also been studied as a building block for the synthesis of complex organic molecules, which can be used in a variety of applications in the field of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 61416-47-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,4,1 and 6 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 61416-47:
(7*6)+(6*1)+(5*4)+(4*1)+(3*6)+(2*4)+(1*7)=105
105 % 10 = 5
So 61416-47-5 is a valid CAS Registry Number.
61416-47-5Relevant academic research and scientific papers
Synthesis of 2-oxazolones and α-aminoketones via palladium-catalyzed reaction of β,β-dibromoenamides
Chai, David I.,Hoffmeister, Laura,Lautens, Mark
supporting information; experimental part, p. 106 - 109 (2011/03/22)
β,β-Dibromoenamides show two different interesting reactivities based on the choice of R group under the reaction conditions. On the basis of mechanistic studies, both reactions proceed via an intermolecular Suzuki-Miyaura C-C coupling and an intramolecular C-O coupling.
