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
This compound 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
This compound 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 articles and documents
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.
