50513-94-5 Usage
Molecular structure
1H-Indeno[1,2-b]pyridine-3-carboxamide, 2,3,4,5-tetrahydro-2-oxo-4-phenylis a complex organic compound that consists of an indeno[1,2-b]pyridine core with a carboxamide group and a tetrahydro-2-oxo-4-phenyl moiety attached to it.
Functional groups
The compound contains a carboxamide group (-CONH2) and a tetrahydro-2-oxo-4-phenyl moiety, which may contribute to its potential pharmacological or biological activities.
Potential pharmacological activities
Due to its unique structure and functional groups, 1H-Indeno[1,2-b]pyridine-3-carboxamide, 2,3,4,5-tetrahydro-2-oxo-4-phenylmay exhibit potential pharmacological or biological activities that could be useful in the development of new drugs or therapies.
Chemical properties and reactivity
The compound's chemical properties and reactivity may make it suitable for various applications in the pharmaceutical or chemical industry, such as the synthesis of new compounds or the development of novel materials.
Need for further research
To fully understand the potential uses and effects of 1H-Indeno[1,2-b]pyridine-3-carboxamide, 2,3,4,5-tetrahydro-2-oxo-4-phenyl-, further research and study are necessary to explore its properties, reactivity, and potential applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 50513-94-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,5,1 and 3 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 50513-94:
(7*5)+(6*0)+(5*5)+(4*1)+(3*3)+(2*9)+(1*4)=95
95 % 10 = 5
So 50513-94-5 is a valid CAS Registry Number.
50513-94-5Relevant academic research and scientific papers
Synthesis of Heterocycles. Part V. (1) The Synthesis of Substituted Indenopyridines
Eweiss, N. F.
, p. 273 - 277 (2007/10/02)
2-Arylmethylene-1-indanones (1) and 2-arylmethylene-1,3-indanediones (VII) react with active methylene compounds in the presence of ammonium acetate as a basic catalyst to afford substituted pyridines.The postulated routes to the formation of the reported
