93951-97-4 Usage
Description
ACENAPHTHYLENE D8, also known as Acenaphthylene (A130750), is a polycyclic aromatic hydrocarbon (PAH) that is labeled with deuterium atoms. It is a type of chemical compound consisting of multiple fused aromatic rings, which can be found in various environmental sources such as coal tar, crude oil, and tobacco smoke. Due to its carcinogenic properties, it has been classified as a potential human carcinogen.
Uses
Used in Environmental and Toxicological Research:
ACENAPHTHYLENE D8 is used as a labeled compound in environmental and toxicological research for studying the behavior, distribution, and effects of PAHs in the environment and on human health. The deuterium labeling allows for easier detection and analysis of the compound in complex samples, providing valuable insights into the mechanisms of PAH-induced toxicity and carcinogenicity.
Used in Cancer Research:
ACENAPHTHYLENE D8 is used as a model compound in cancer research to investigate the molecular mechanisms underlying the carcinogenic effects of PAHs. By studying the interactions of ACENAPHTHYLENE D8 with cellular macromolecules, researchers can gain a better understanding of the pathways and processes involved in PAH-induced carcinogenesis, potentially leading to the development of new strategies for cancer prevention and treatment.
Used in Analytical Chemistry:
ACENAPHTHYLENE D8 is used as an internal standard or a reference compound in analytical chemistry for the quantification and identification of PAHs in various samples, such as air, water, soil, and biological tissues. The deuterium labeling provides a distinct mass signature, enabling accurate and reliable measurements of PAH concentrations and facilitating the assessment of exposure risks and environmental contamination.
Used in Pharmaceutical Development:
ACENAPHTHYLENE D8 can be used in pharmaceutical development as a starting material or a structural analog for the synthesis of novel compounds with potential therapeutic applications. By understanding the chemical properties and biological activities of ACENAPHTHYLENE D8, researchers can design and develop new drugs with improved efficacy and reduced toxicity.
Check Digit Verification of cas no
The CAS Registry Mumber 93951-97-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,9,5 and 1 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 93951-97:
(7*9)+(6*3)+(5*9)+(4*5)+(3*1)+(2*9)+(1*7)=174
174 % 10 = 4
So 93951-97-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H8/c1-3-9-4-2-6-11-8-7-10(5-1)12(9)11/h1-8H/i1D,2D,3D,4D,5D,6D,7D,8D
93951-97-4Relevant articles and documents
Formation of an atomically abrupt interface between a polycyclic aromatic molecule and the silicon (001) surface via direct Si-C linkage
Schwartz, Michael P.,Halter, Robert J.,McMahon, Robert J.,Hamers, Robert J.
, p. 224 - 228 (2003)
The reaction of acenaphthylene with the Si(001) surface has been investigated as a model system for understanding how complex ??-systems interact with a ??-bonded semiconductor surface. Scanning tunneling microscopy (STM) reveals that bonding occurs over a dimer row for more than 90% of the adsorbed molecules. Fourier transform infrared spectroscopy (FTIR), using isotopically labeled derivatives of acenaphthylene, shows that bonding occurs through the 1,2-alkene, leaving the aromatic portion of the molecule mostly unperturbed. The reaction between acenaphthylene and Si(001) represents a potential method for coupling extended ??-electron systems with group IV semiconductor surfaces.
