60847-47-4 Usage
Heterocyclic compound
Five-membered ring with nitrogen and oxygen atoms
The compound has a five-membered ring structure that includes both nitrogen and oxygen atoms, making it a heterocyclic compound.
Common usage
Chemical and pharmaceutical research
2,3-Dihydro-2-oxo-1-indolizinecarbonitrile is frequently used in research related to chemistry and pharmaceuticals, contributing to the development of new drugs and materials.
Potential applications
Drug development and material science
Due to its unique properties, the compound has potential applications in creating new drugs and materials, making it a valuable asset in these fields.
Biological activities and therapeutic effects
Studied for its potential benefits
The compound has been researched for its biological activities and possible therapeutic effects, making it an important focus for the pharmaceutical industry.
Unique chemical structure
A subject of interest for various fields
The distinctive chemical structure and properties of 2,3-Dihydro-2-oxo-1-indolizinecarbonitrile make it an intriguing subject for research and development in multiple areas.
Check Digit Verification of cas no
The CAS Registry Mumber 60847-47-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,8,4 and 7 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 60847-47:
(7*6)+(6*0)+(5*8)+(4*4)+(3*7)+(2*4)+(1*7)=134
134 % 10 = 4
So 60847-47-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H6N2O/c10-5-7-8-3-1-2-4-11(8)6-9(7)12/h1-4H,6H2
60847-47-4Relevant academic research and scientific papers
Reaction of 2-(2-azahetaryl)-4-chloro-3-oxobutyronitriles with substituted benzaldehyde hydrazones. Unexpected formation of 4-arylideneamino-2-(1-R-benzimidazol-2-YL)-3-oxobutyronitriles
Volovenko,Tverdokhlebov,Volovnenko
, p. 876 - 884 (2007/10/03)
The reaction of 2-(2-azahetaryl)-3-oxo-4-chlorobutyronitriles with substituted benzaldehyde hydrazones gives 4-arylideneamino-2-(1-R-benzimidazol-2-yl)-3-oxobutyronitriles, the structures of which were proved using spectroscopic data, the results of elemental analysis, and through their chemical reactions. It was found that the reaction course depends on the basicity of the heterocyclic fragment in the starting nitrile. A likely mechanism for the process is proposed.
