102420-56-4 Usage
Uses
Given the provided materials, there are no specific applications listed for (11R,12R)-11,12-dihydroindeno[1,2,3-cd]pyrene-11,12-diol. The information focuses on its environmental impact and health risks. However, in a broader context, understanding the properties of such compounds is crucial for developing methods to detect, mitigate, and manage their presence in the environment. This could involve:
1. Environmental Monitoring:
(11R,12R)-11,12-dihydroindeno[1,2,3-cd]pyrene-11,12-diol is used as a target analyte for environmental monitoring to assess pollution levels and human exposure risks.
2. Research and Development:
In the field of environmental chemistry and toxicology, (11R,12R)-11,12-dihydroindeno[1,2,3-cd]pyrene-11,12-diol serves as a subject for research to understand its mechanisms of action, effects on ecosystems, and potential mitigation strategies.
3. Regulatory Compliance:
It is utilized in regulatory frameworks as a parameter to ensure compliance with environmental safety standards and to guide the development of policies aimed at reducing the emission of such harmful substances.
4. Public Health Education:
Information about (11R,12R)-11,12-dihydroindeno[1,2,3-cd]pyrene-11,12-diol is used in public health initiatives to educate communities about the risks associated with environmental pollutants and the importance of a clean environment for health and well-being.
Check Digit Verification of cas no
The CAS Registry Mumber 102420-56-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,4,2 and 0 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 102420-56:
(8*1)+(7*0)+(6*2)+(5*4)+(4*2)+(3*0)+(2*5)+(1*6)=64
64 % 10 = 4
So 102420-56-4 is a valid CAS Registry Number.
102420-56-4Relevant academic research and scientific papers
Synthesis of Oxygenated Metabolites of Indenopyrene
Rice, Joseph E.,LaVoie, Edmond J.
, p. 2428 - 2434 (2007/10/02)
The syntheses of cis- and trans-1,2-dihydro-1,2-dihydroxyindenopyrene, 1,2-dihydroindenopyrene 1,2-epoxide, and 1-, 2-, 6-, 7-, 8-, 9-, and 10-hydroxyindenopyrene are described.UV and high-resolution NMR spectral data are rep
