5212-66-8 Usage
Uses
Used in Chemical Synthesis:
2,3,4,5,6-pentafluoro-N-phenylbenzamide is utilized as a building block in the synthesis of other organic molecules. Its structural features allow it to serve as a key intermediate in the creation of more complex chemical entities, contributing to the diversity of organic chemistry.
Used in Pharmaceutical Development:
2,3,4,5,6-pentafluoro-N-phenylbenzamide is employed in the pharmaceutical industry as a potential candidate for drug development. Its ability to interact with biological systems suggests that it could be instrumental in the formulation of new drugs, particularly those targeting specific biological pathways or receptors.
Used in Catalysts and Reagents:
2,3,4,5,6-pentafluoro-N-phenylbenzamide also finds application in the role of a catalyst or reagent in various chemical reactions. Its unique properties can influence the rate and outcome of reactions, making it a valuable asset in the field of catalysis and synthetic chemistry.
Used in Research and Development:
In the context of research and development, 2,3,4,5,6-pentafluoro-N-phenylbenzamide is used to explore new chemical reactions, investigate its potential as a pharmaceutical agent, and understand its interactions with biological systems. 2,3,4,5,6-pentafluoro-N-phenylbenzamide serves as a test subject for advancing knowledge in both chemistry and medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 5212-66-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,1 and 2 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5212-66:
(6*5)+(5*2)+(4*1)+(3*2)+(2*6)+(1*6)=68
68 % 10 = 8
So 5212-66-8 is a valid CAS Registry Number.
5212-66-8Relevant academic research and scientific papers
Oxidation of 1-hydroxyazetidines to four-membered cyclic nitrones and β-lactams
Elburg, P. A. van,Reinhoudt, D. N.
, p. 381 - 387 (2007/10/02)
The 1-(benzyloxy)azetidines 7a-c and 16a,b were synthesized by reductive cyclization of the corresponding oximes 5a-c and 14a-d.Oxidation of the 1-hydroxyazetidines 8a-c and 17 with PbO2 afforded the corresponding four-membered cyclic nitrones 18a-c and t
