94064-79-6 Usage
Indene derivative
Indene class of organic compounds 1-oxo-3-phenyl-1H-indene-2-carboxamide belongs to the indene class of organic compounds, which are derivatives of the parent compound indene.
Carbonyl group
Presence of a carbon-oxygen double bond (C=O) This compound contains a carbonyl group, which is a functional group consisting of a carbon-oxygen double bond.
Amide group
Presence of a nitrogen-oxygen single bond (N-O) 1-oxo-3-phenyl-1H-indene-2-carboxamide contains an amide group, which is a functional group consisting of a nitrogen-oxygen single bond.
Phenyl group
Presence of a six-membered aromatic ring (C6H5) This compound also contains a phenyl group, which is a six-membered aromatic ring with five hydrogen atoms and one carbon atom.
Potential applications
Medicinal chemistry and drug development Due to its structural features and potential biological activities, 1-oxo-3-phenyl-1H-indene-2-carboxamide may have potential applications in the field of medicinal chemistry and drug development.
Further research needed
Exploration of properties and potential uses Additional research and studies are required to fully understand the range of properties and potential uses of 1-oxo-3-phenyl-1H-indene-2-carboxamide.
Check Digit Verification of cas no
The CAS Registry Mumber 94064-79-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,0,6 and 4 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 94064-79:
(7*9)+(6*4)+(5*0)+(4*6)+(3*4)+(2*7)+(1*9)=146
146 % 10 = 6
So 94064-79-6 is a valid CAS Registry Number.
94064-79-6Relevant articles and documents
FeCl3 mediated synthesis of substituted indenones by a formal [2+2] cycloaddition/ring opening cascade of o-keto-cinnamates
Dethe, Dattatraya H.,Murhade, Ganesh M.
, p. 10891 - 10894 (2015/06/30)
A novel FeCl3 mediated formal [2+2] cycloaddition/ring opening cascade of o-keto-cinnamates was developed for the synthesis of indenones. The reaction tolerates a broad range of functional groups, including bromide, chloride, amide, acid and es
