116-96-1 Usage
Uses
Given the highly toxic and carcinogenic nature of [3,3'-Bi-7H-benz[de]anthracene]-7,7'-dione, its uses are primarily focused on research and regulatory efforts to mitigate its harmful effects. However, it is important to note that the compound itself is not intentionally used in any applications due to its hazardous properties. Instead, the focus is on:
1. Environmental Monitoring:
[3,3'-Bi-7H-benz[de]anthracene]-7,7'-dione is monitored as a pollutant in environmental samples to assess the level of contamination in air, water, and soil, particularly in areas with high industrial activity or cigarette smoke exposure.
2. Regulatory Compliance:
It is used as a reference substance in setting regulatory standards and guidelines for permissible exposure levels in various industries to ensure public health and safety.
3. Toxicological Research:
[3,3'-Bi-7H-benz[de]anthracene]-7,7'-dione serves as a subject in toxicological studies to understand its mechanisms of action, metabolic pathways, and potential interactions with biological systems, which can aid in developing strategies for risk assessment and mitigation.
4. Cancer Research:
It is utilized in cancer research to investigate the molecular and cellular effects of exposure to this carcinogen, providing insights into the development of cancer and potential therapeutic interventions.
5. Public Health Education:
[3,3'-Bi-7H-benz[de]anthracene]-7,7'-dione is referenced in public health campaigns to raise awareness about the dangers of exposure to carcinogenic substances found in cigarette smoke, industrial emissions, and grilled or charred foods.
Check Digit Verification of cas no
The CAS Registry Mumber 116-96-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,1 and 6 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 116-96:
(5*1)+(4*1)+(3*6)+(2*9)+(1*6)=51
51 % 10 = 1
So 116-96-1 is a valid CAS Registry Number.
116-96-1Relevant academic research and scientific papers
Perylene derivatives formation in reaction of 3-bromobenzanthrone and 4-bromonaphthalic acid derivatives with a reduction system NiCl2 - 2,2′bipyridyl (or 1,10-phenathroline) - Zn
Adonin,Ryabinin,Starichenko
, p. 861 - 865 (2007/10/03)
The reaction of 3-bromobenzanthrone and 4-bromonaphthalic acid derivatives with a reduction system NiCl2-2,2′bipyridyl (or 1,10-phenathroline)-Zn gives rise to compounds containing perylene fragment. Under similar conditions was established a possibility to transform substituted 1,1′-binaphthyls into the corresponding perylene derivatives.
ELECTRONIC STRUCTURE OF ?-SYSTEMS. XII. THE BENZANTHRONE RADICAL CATION
Safronov, A. I.,Makarov, I. G.,Kazakova, V. M.,Chibisova, T. A.,Traven', V. F.
, p. 2112 - 2115 (2007/10/02)
ESR spectroscopy was used to show that the benzanthrone radical cation is formed upon the action of strong oxidizing agents on a solution of benzanthrone in concentrated sulfuric acid.The benzanthrone radical cation has maximum spin density at C3.Subsequent dimerization occurs at this position with the formation of 3,3'-dibenzanthronyl.
