32795-84-9 Usage
Uses
Used in Laboratory Research:
7-Bromobenz[a]anthracene is used as a research tool for inducing tumors in animals, serving as a valuable asset in studying the mechanisms of carcinogenesis. Its ability to induce tumors makes it instrumental in understanding how cancer develops and progresses, which is crucial for developing potential treatments and preventive measures.
Used in Toxicological Studies:
Due to its potential harmful effects on human health, 7-Bromobenz[a]anthracene is used in toxicological studies to investigate the risks associated with exposure to PAHs. These studies aim to determine the extent of the compound's impact on reproductive and developmental toxicity, as well as its contribution to the increased risk of cancer.
Used in Environmental Monitoring:
Given the link between PAHs and adverse health effects, 7-Bromobenz[a]anthracene can be used in environmental monitoring programs to assess the presence and concentration of such compounds in various ecosystems. This helps in evaluating the potential risks to both human health and the environment, guiding the development of strategies to mitigate exposure.
Used in Chemical Synthesis:
As a halogenated derivative of benz[a]anthracene, 7-Bromobenz[a]anthracene may also find applications in chemical synthesis processes, particularly in the development of new compounds with specific properties. Its unique structure and reactivity can be leveraged to create novel molecules for various applications, including pharmaceuticals and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 32795-84-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,7,9 and 5 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 32795-84:
(7*3)+(6*2)+(5*7)+(4*9)+(3*5)+(2*8)+(1*4)=139
139 % 10 = 9
So 32795-84-9 is a valid CAS Registry Number.
32795-84-9Relevant academic research and scientific papers
Cascade reaction for the synthesis of polycyclic aromatic hydrocarbons via transient directing group strategy
Wang, Ziqi,Dong, Wendan,Sun, Bing,Yu, Qinqin,Zhang, Fang-Lin
, p. 4031 - 4041 (2019/07/03)
A Pd(II)-catalyzed cascade synthesis of diverse polycyclic aromatic hydrocarbons via transient directing group strategy has been developed, involving the consecutive arylation, cyclization and aromatization. The efficiency and practicality were demonstrated by wide substrate range, concise synthetic pathway and mild reaction conditions. The subsequent transformations of the benz[a]anthracene core accessed natural bioactive PAH molecules.
Reactions of (η6-Arene)tricarbonylchromium Complexes: Hydrogenation, Nitration, and Bromination
Own
, p. 417 - 423 (2007/10/03)
In this study, we explore the reactions of coordinated arenes, e.g., hydrogenation, nitration, and bromination, to prepare compounds which are not accessible from conventional organic synthesis. The reaction products formed from reactions with the coordinated and the uncoordinated arenes are compared. The polycyclic aromatic hydrocarbons (PAHs) employed for this study include phenanthrene, methyl- and acetyl-phenanthrene, and benz[a]anthracene (BA). The tricarbonylchromium group demonstrated various characteristics which influence the reactions in this work, such as an electronic effect to deactivate hydrogenation, a steric effect to exhibit highly positional selective nitration, and a free radical mechanism to direct bromine to attack at the ring coordinated to tricarbonylchromium.
