15254-64-5 Usage
Uses
Given the provided materials, there are no direct applications listed for 2,4-DIMETHYLPHENANTHRENE. However, it is important to note that due to its carcinogenic properties, efforts are focused on reducing its presence in the environment and minimizing exposure to this chemical compound. The primary use in this context would be in research aimed at understanding its effects and developing methods for its detection, monitoring, and mitigation in various industries, such as:
Used in Environmental Research and Monitoring:
2,4-DIMETHYLPHENANTHRENE is used as a subject of study for understanding its environmental impact and health risks, with the aim of developing strategies for its reduction and control in polluted areas.
Used in Regulatory Compliance:
2,4-DIMETHYLPHENANTHRENE is used as a parameter in regulatory frameworks to ensure that industries adhere to emission standards and take necessary measures to minimize the release of this harmful compound into the environment.
Used in Public Health Initiatives:
2,4-DIMETHYLPHENANTHRENE is used as a reference in public health campaigns to raise awareness about the dangers of exposure to environmental pollutants and the importance of adopting healthier lifestyles and practices to reduce exposure risks.
Check Digit Verification of cas no
The CAS Registry Mumber 15254-64-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,2,5 and 4 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 15254-64:
(7*1)+(6*5)+(5*2)+(4*5)+(3*4)+(2*6)+(1*4)=95
95 % 10 = 5
So 15254-64-5 is a valid CAS Registry Number.
InChI:InChI=1/C16H14/c1-11-9-12(2)16-14(10-11)8-7-13-5-3-4-6-15(13)16/h3-10H,1-2H3
15254-64-5Relevant academic research and scientific papers
Regioselective Synthesis of Polycyclic and Heptagon-embedded Aromatic Compounds through a Versatile π-Extension of Aryl Halides
Fu, Wai Chung,Wang, Zheng,Chan, Wesley Ting Kwok,Lin, Zhenyang,Kwong, Fuk Yee
supporting information, p. 7166 - 7170 (2017/06/13)
A versatile π-extension reaction was developed based on the three-component cross-coupling of aryl halides, 2-haloarylcarboxylic acids, and norbornadiene. The transformation is driven by the direction and subsequent decarboxylation of the carboxyl group, while norbornadiene serves as an ortho-C?H activator and ethylene synthon via a retro-Diels–Alder reaction. Comprehensive DFT calculations were performed to account for the catalytic intermediates.
