6815-85-6 Usage
Uses
Used in Research Applications:
2,2'-Biphenanthrene is used as a research compound for studying the properties and effects of polycyclic aromatic hydrocarbons. It serves as a model compound to understand the behavior of similar molecules in various chemical and environmental contexts.
Used in Analytical Chemistry:
In the field of analytical chemistry, 2,2'-Biphenanthrene is used as a reference standard. It helps in the calibration of instruments and the development of analytical methods for detecting and quantifying PAHs in samples.
Used in Environmental Monitoring:
2,2'-Biphenanthrene is used as an indicator of environmental pollution, particularly in soil and groundwater. Its presence can signal the contamination by coal tar and other fossil fuels, which is important for assessing the quality of the environment and the potential health risks associated with exposure to these pollutants.
Used in Toxicological Studies:
Due to its potential carcinogenic and mutagenic properties, 2,2'-Biphenanthrene is used in toxicological studies to investigate the mechanisms of action and the effects of exposure to PAHs on human health. This research is crucial for developing strategies to mitigate the risks associated with these compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 6815-85-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,1 and 5 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6815-85:
(6*6)+(5*8)+(4*1)+(3*5)+(2*8)+(1*5)=116
116 % 10 = 6
So 6815-85-6 is a valid CAS Registry Number.
6815-85-6Relevant academic research and scientific papers
OXIDATIVE COUPLING OF 9,10-DIHYDROPHENANTHRENE AND POLYNUCLEAR HYDROCARBONS BY ALUMINUM CHLORIDE-CUPRIC CHLORIDE
Guenther, Howard,Kovacic, Peter
, p. 413 - 428 (2007/10/02)
Products from the oxidative coupling of 9,10-dihydrophenanthrene and polynuclear hydrocarbons (phenanthrene and pyrene) with AlCl3-CuCl2 included the respective dehydro dimers and trimers, accompanied by higher oligomers.
