7229-88-1 Usage
General Description
7,14-diphenylacenaphtho[1,2-k]fluoranthene is a polycyclic aromatic hydrocarbon (PAH) chemical compound consisting of 20 carbon atoms arranged in a complex ring structure. It is a known environmental pollutant and is classified as a potential human carcinogen. It is formed as a byproduct of incomplete combustion and is found in coal tar, cigarette smoke, and vehicle exhaust. 7,14-diphenylacenaphtho[1,2-k]fluoranthene is also produced through industrial processes such as the burning of fossil fuels and the production of coke and aluminum. Exposure to this compound has been linked to adverse health effects, including respiratory issues and cancer. Its persistence in the environment and potential for bioaccumulation make it a cause for concern in environmental and public health.
Check Digit Verification of cas no
The CAS Registry Mumber 7229-88-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,2 and 9 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7229-88:
(6*7)+(5*2)+(4*2)+(3*9)+(2*8)+(1*8)=111
111 % 10 = 1
So 7229-88-1 is a valid CAS Registry Number.
7229-88-1Relevant articles and documents
Synthesis of fluoranthenes and indenocorannulenes: Elucidation of chiral stereoisomers on the basis of static molecular bowls
Wu, Yao-Ting,Hayama, Tomoharu,Baldridge, Kim K.,Linden, Anthony,Siegel, Jay S.
, p. 6870 - 6884 (2007/10/03)
Cycloaromatization of a peri diyne with an external alkyne provides a general route to indenofused polynuclear aromatics. Fluoranthenes 9 (or 13) are easily accessible in good to excellent yields (75-99%; 18 examples) from the reaction of symmetric (or as
Verwendung von Bis(1,2,4,6-tetramethyl-1,4-dihydro-4-pyridinyl) als Reduktionsmittel zur Erzeugung organischer Radikalanionen fuer EPR-Spektroskopie
Pragst, Fritz,Stoesser, Reinhard
, p. 222 (2007/10/02)
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