67976-99-2 Usage
Chemical Class
Polycyclic aromatic hydrocarbon (PAH)
Mutagenic Properties
Potent mutagen
Carcinogenic Properties
Potent carcinogen
Cancer Risk
High risk of developing cancer, particularly in the respiratory system
Toxicity
Highly toxic
Tumor Induction
Known to induce tumors in experimental animals
Cytochrome P450 Enzyme Induction
Potent inducer of cytochrome P450 enzymes
Metabolic Activation
Plays a key role in the metabolic activation of many environmental carcinogens
Environmental Pollutant
Commonly found in certain types of coal and released into the environment during the combustion of fossil fuels
Human Health Risk
Poses a significant risk to human health
Environmental Risk
Poses a significant risk to the environment
Check Digit Verification of cas no
The CAS Registry Mumber 67976-99-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,9,7 and 6 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 67976-99:
(7*6)+(6*7)+(5*9)+(4*7)+(3*6)+(2*9)+(1*9)=202
202 % 10 = 2
So 67976-99-2 is a valid CAS Registry Number.
67976-99-2Relevant academic research and scientific papers
Mono-, and Dibenzacridine Imines. Synthesis of 1a,11b-Dihydrobenzazirinoacridine, 4b,5a-Dihydrodibenzazirinoacridine and 1a,13b-Dihydrodibenzazirinoacridine
Bazanov, Nina,Dayan, Yael,Blum, Jochanan,Harvey, Ronald G.
, p. 837 - 840 (2007/10/02)
The syntheses of the K-imine derivatives of benzacridine, dibenzacridine and dibenzacridine are described.The parent hydrocarbons 1, 6 and 11 were oxidized with sodium hypochlorite under phase transfer conditions to the corresponding K-oxides 4, 9 and 14, which in turn were reacted with sodium azide.The resulting azido alcohols were then cyclized with tributylphosphine to the title compounds 5, 10 and 15.
