215-62-3 Usage
Uses
Used in Environmental Monitoring:
Dibenzo(a,c)acridine is used as a biomarker for assessing the presence of environmental pollutants, particularly in air, water, and soil. Monitoring its levels helps in understanding the extent of pollution and the effectiveness of measures taken to reduce emissions and exposure.
Used in Research and Toxicology Studies:
Dibenzo(a,c)acridine serves as a subject in research and toxicology studies aimed at understanding its carcinogenic properties, mechanisms of action, and potential health risks associated with exposure. This research is crucial for developing strategies to mitigate its harmful effects and for regulatory purposes.
Used in Regulatory Frameworks:
Dibenzo(a,c)acridine is a key compound in the development of regulatory frameworks and guidelines for controlling emissions from various sources, such as tobacco smoke and industrial processes. Its inclusion in these frameworks helps in minimizing exposure and reducing its environmental presence.
Efforts to minimize exposure to dibenzo(a,c)acridine and reduce its environmental presence are ongoing, with a particular emphasis on the regulation of smoking and industrial emissions.
Check Digit Verification of cas no
The CAS Registry Mumber 215-62-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,1 and 5 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 215-62:
(5*2)+(4*1)+(3*5)+(2*6)+(1*2)=43
43 % 10 = 3
So 215-62-3 is a valid CAS Registry Number.
InChI:InChI=1/C21H13N/c1-6-12-20-14(7-1)13-19-17-10-3-2-8-15(17)16-9-4-5-11-18(16)21(19)22-20/h1-13H
215-62-3Relevant academic research and scientific papers
Et3SiH + KO: T Bu provide multiple reactive intermediates that compete in the reactions and rearrangements of benzylnitriles and indolenines
Arokianathar, Jude N.,Clark, Kenneth F.,Dimitrova, Daniela,Leach, Stuart G.,Murphy, John A.,Poole, Darren L.,Smith, Andrew J.
, p. 12364 - 12370 (2020/12/08)
The combination of potassium tert-butoxide and triethylsilane is unusual because it generates multiple different types of reactive intermediates simultaneously that provide access to (i) silyl radical reactions, (ii) hydrogen atom transfer reactions to cl
Gold-Catalyzed Regiospecific C?H Annulation of o-Ethynylbiaryls with Anthranils: π-Extension by Ring-Expansion En Route to N-Doped PAHs
Zeng, Zhongyi,Jin, Hongming,Sekine, Kohei,Rudolph, Matthias,Rominger, Frank,Hashmi, A. Stephen K.
supporting information, p. 6935 - 6939 (2018/06/04)
We describe a novel, short, and flexible approach to diverse N-doped polycyclic aromatic hydrocarbons (PAHs) through gold-catalyzed π-extension of anthranils with o-ethynylbiaryls as reagents. This strategy uses easily accessible starting materials, is simple due to high step and atom economy, and shows good functional-group compatibility as well as scale-up potential. Mechanistically, the tandem reaction is proposed to involve a nucleophilic addition/ring opening/regiospecific C?H annulation/protodeauration sequence terminated by a Friedel–Crafts-type cyclization. Photophysical studies of the products indicated violet-blue fluorescence emission with quantum yields up to 0.45.
