58963-35-2 Usage
Chemical structure
Ketone with an indolizine ring and a chloro-phenyl group
The compound features a carbonyl group (C=O) and an indolizine ring, which is a seven-membered nitrogen-containing heterocycle. Additionally, it has a chloro-phenyl group attached to the indolizine ring.
Potential applications
Pharmaceuticals, research, and organic synthesis
Due to its unique structure and potential biological activities, 1-[2-(4-CHLORO-PHENYL)-INDOLIZIN-3-YL]-ETHANONE may be useful in the development of new drugs, as a research tool, or in organic synthesis processes.
Biological activities
Unknown at this time
Further studies are needed to determine the specific biological activities and potential therapeutic effects of 1-[2-(4-CHLORO-PHENYL)-INDOLIZIN-3-YL]-ETHANONE.
Risks
Unknown at this time
More research is required to understand the potential risks associated with handling and exposure to 1-[2-(4-CHLORO-PHENYL)-INDOLIZIN-3-YL]-ETHANONE.
Further studies needed
To determine specific properties, uses, and potential risks
Additional research is necessary to fully understand the properties, applications, and safety of 1-[2-(4-CHLORO-PHENYL)-INDOLIZIN-3-YL]-ETHANONE.
Check Digit Verification of cas no
The CAS Registry Mumber 58963-35-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,9,6 and 3 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 58963-35:
(7*5)+(6*8)+(5*9)+(4*6)+(3*3)+(2*3)+(1*5)=172
172 % 10 = 2
So 58963-35-2 is a valid CAS Registry Number.
InChI:InChI=1/C16H12ClNO/c1-11(19)16-15(12-5-7-13(17)8-6-12)10-14-4-2-3-9-18(14)16/h2-10H,1H3
58963-35-2Relevant academic research and scientific papers
The first approach to the synthesis of 1-unsubstituted 2- arylindolizines by intramolecular 1,5-dipolar cyclization of 2-(2- arylethenyl)pyridinium ylides in the presence of tetrakis(pyridine)cobalt (II) dichromate
Zhou, Jian,Yuefei, Hu,Hongwen, Hu
, p. 166 - 170 (2007/10/03)
The first approach to the preparation of 1-unsubstituted 2- arylindolizines by intramolecular 1,5-dipolar cyclization of 2-(2- arylethenyl)pyridinium ylides 2a-v in the presence of tetrakis(pyridine)cobalt (II) dichromate was developed. Several kinds of n
