2541-69-7 Usage
Description
7-METHYLBENZ[A]ANTHRACENE, also known as a monomethylated polycyclic aromatic hydrocarbon, is a chemical compound with carcinogenic activity. It is characterized by its complex ring structure and the presence of a methyl group attached to the benzene ring.
Uses
Used in Research and Development:
7-METHYLBENZ[A]ANTHRACENE is used as a research compound for studying the effects of carcinogens on biological systems. Its carcinogenic properties make it a valuable tool in understanding the mechanisms of cancer development and the potential for developing new treatments or preventive measures.
Used in Environmental Monitoring:
7-METHYLBENZ[A]ANTHRACENE is used as a marker for environmental contamination, particularly in the context of air and water pollution. Its presence can indicate the presence of other harmful substances, allowing for better assessment of environmental risks and the implementation of appropriate mitigation strategies.
Used in Industrial Applications:
In some industries, 7-METHYLBENZ[A]ANTHRACENE may be used as an intermediate in the synthesis of various chemicals and materials. However, due to its carcinogenic nature, its use in these applications is carefully regulated to minimize potential health risks.
Check Digit Verification of cas no
The CAS Registry Mumber 2541-69-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,4 and 1 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2541-69:
(6*2)+(5*5)+(4*4)+(3*1)+(2*6)+(1*9)=77
77 % 10 = 7
So 2541-69-7 is a valid CAS Registry Number.
2541-69-7Relevant articles and documents
Aldimine-directed branched-selective hydroarylation of styrenes
Lee, Pin-Sheng,Yoshikai, Naohiko
, p. 1240 - 1244 (2013/03/13)
Branching out: A simple and inexpensive cobalt/triarylphosphine catalyst promotes aldimine-directed hydroarylation of styrene with high branched regioselectivity to afford 1,1-diarylethane derivatives in good yields under mild reaction conditions. The ortho-formyl group in the hydroarylation products is amenable to dehydrative cyclization, to give fused polycyclic aromatic hydrocarbons, as well as decarbonylative removal. Copyright
SYNTHESIS OF 3-METHYLCHOLANTHRENE
Jacobs, Stephen A.,Harvey, Ronald G.
, p. 1093 - 1096 (2007/10/02)
A novel synthesis of 3-methylcholanthrene is described which is operationally simpler than the method in current use and is potentially applicable to the synthesis of a wide range of other polycyclic hydrocarbons and their oxidized carcinogenic metabolites.
