4985-70-0 Usage
Description
1-Chloroanthracene is a polycyclic aromatic hydrocarbon that forms a photodimer called trans-bi(1-chloro-9,10-dihydro-9,10-anthracenediyl) through the solid-state [4+4]-photodimerization process. It is known for its potential applications in various fields due to its unique chemical properties.
Uses
Used in Research Applications:
1-Chloroanthracene is used as a research compound for investigating the effects of polycyclic aromatic hydrocarbons on gap junctional intercellular communication and the activation of intracellular receptor kinase in F344 rat liver epithelial cells. This application helps in understanding the interactions and potential impacts of these chemicals on cellular processes and communication.
Used in Chemical Synthesis:
1-Chloroanthracene can be used as a starting material or intermediate in the synthesis of various organic compounds, particularly those involving polycyclic aromatic structures. Its unique chemical properties make it a valuable component in the development of new molecules with specific applications in different industries.
Used in Environmental Studies:
1-Chloroanthracene can be employed in environmental studies to understand the behavior and impact of polycyclic aromatic hydrocarbons in the environment. This knowledge can contribute to the development of strategies for pollution control and remediation efforts.
Used in Pharmaceutical Research:
Although not explicitly mentioned in the provided materials, 1-chloroanthracene may have potential applications in the pharmaceutical industry as a compound for the development of new drugs or drug candidates. Its unique chemical structure could be utilized in the design of novel therapeutic agents targeting specific biological pathways or receptors.
Synthesis Reference(s)
The Journal of Organic Chemistry, 51, p. 1914, 1986 DOI: 10.1021/jo00360a054
Check Digit Verification of cas no
The CAS Registry Mumber 4985-70-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,8 and 5 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4985-70:
(6*4)+(5*9)+(4*8)+(3*5)+(2*7)+(1*0)=130
130 % 10 = 0
So 4985-70-0 is a valid CAS Registry Number.
InChI:InChI=1/C14H9Cl/c15-14-7-3-6-12-8-10-4-1-2-5-11(10)9-13(12)14/h1-9H
4985-70-0Relevant articles and documents
Efficient indium-mediated dehalogenation of aromatics in ionic liquid media
Canete, Alvaro F.,Salas, Cristian O.,Zacconi, Flavia C.
, p. 398 - 407 (2013/03/13)
An efficient indium-mediated dehalogenation reaction of haloaromatics and haloheteroaromatics in ionic liquids has been studied. This method is simple and effective in the presence of [bmim]Br. Furthermore, this methodology is environmentally friendly compared with conventional ones.
Benzannulated Isobenzofurans
Moursounidis, John,Wege, Dieter
, p. 235 - 249 (2007/10/02)
A number of arynes, generated by treatment of haloarenes with sodium or potassium amide in tetrahydrofuran, were trapped with furan.The resulting dihydro epoxy arenes were converted into the following annulated isobenzofuran derivatives by using reverse Diels-Alder methodology: naphthofuran, phenanthrofuran, pyrenofuran, pyrenofuran, anthrafuran, phenanthrofuran and phenathrofuran.Bimolecular rate constants for the addition of maleic anhydride to these furans were measured, and were correlated with the Herndon structure count.Addition of arynes to selected members of this furan series yielded adducts which were deoxygenated to afford polycyclic aromatic hydrocarbons.
Anomalous Course of Leuckart Reduction of Anthraquinones by Formamide
Flemming, Cecily A.,Gibson, Martin S.,Kaldas, Magdy L.
, p. 378 - 379 (2007/10/02)
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