861242-82-2 Usage
Uses
Used in Coordination Chemistry:
3-bromo-1,10-phenanthroline-5,6-dione is used as a ligand in coordination chemistry for forming complexes with metal ions. Its ability to chelate metals allows for the study of metal ion properties and the development of new coordination compounds.
Used in Organic Synthesis:
In the field of organic synthesis, 3-bromo-1,10-phenanthroline-5,6-dione is used as a building block or intermediate for the synthesis of various organic compounds. Its reactivity and structural features make it a valuable component in the creation of complex organic molecules.
Used in Chemical Analysis:
3-bromo-1,10-phenanthroline-5,6-dione is utilized as a reagent in chemical analysis for the detection and quantification of specific analytes. Its chemical properties enable selective reactions with target compounds, facilitating their identification and measurement.
Used in Antitumor Applications:
3-bromo-1,10-phenanthroline-5,6-dione is studied for its potential as an antitumor agent, with research focusing on its ability to inhibit tumor growth and proliferation. Its mechanism of action and potential synergistic effects with other therapeutic agents are of interest in the development of novel cancer treatments.
Used in Antibacterial Applications:
3-bromo-1,10-phenanthroline-5,6-dione is also explored for its antibacterial properties, with potential use in the development of new antimicrobial agents. Its ability to target and inhibit bacterial growth could contribute to the fight against antibiotic-resistant strains.
Used in Fluorescent Labeling and Imaging Studies:
Due to its fluorescent properties, 3-bromo-1,10-phenanthroline-5,6-dione is used as a fluorescent label in biological and chemical imaging studies. Its ability to emit light upon excitation allows for the visualization and tracking of specific molecules or cellular structures, aiding in research and diagnostics.
Used in Research and Industry:
3-bromo-1,10-phenanthroline-5,6-dione's diverse applications in coordination chemistry, organic synthesis, chemical analysis, antitumor and antibacterial studies, and fluorescent labeling make it a valuable compound in both research and industry settings. Its unique properties and potential uses contribute to the advancement of scientific knowledge and the development of new technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 861242-82-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,1,2,4 and 2 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 861242-82:
(8*8)+(7*6)+(6*1)+(5*2)+(4*4)+(3*2)+(2*8)+(1*2)=162
162 % 10 = 2
So 861242-82-2 is a valid CAS Registry Number.
861242-82-2Relevant articles and documents
Oxidation for unsymmetrical bromo-1,10-phenanthrolines and subsequent hydroxylation, decarbonylation and chlorination reactions
Peng, Yu-Xin,Hu, Bin,Huang, Wei
, p. 4495 - 4503 (2018/07/21)
A systematic investigation on the oxidation of unsymmetric bromo-phens is presented herein, where the reaction temperature is found to be the key parameter to generate oxidation or oxidation-bromination products. The regioselective C3-brominated compounds are produced in moderate yields in the cases of 2-bromo-phen and 4-bromo-phen. Subsequent hydroxylation and decarbonylation for bromo-phds are also studied, where a series of bromo-diazafluorenones and phen-triones have been isolated. Furthermore, various chlorination products have been obtained by treating bromo-phds or bromo-phts with excess POCl3.
One-pot synthesis of 2-bromo-4,5-diazafluoren-9-one via a tandem oxidation-bromination-rearrangement of phenanthroline and its hammer-shaped donor-acceptor organic semiconductors
Zhao, Jian-Feng,Chen, Lin,Sun, Peng-Ju,Hou, Xiao-Ya,Zhao, Xiang-Hua,Li, Wei-Jie,Xie, Ling-Hai,Qian, Yan,Shi, Nai-En,Lai, Wen-Yong,Fan, Qu-Li,Huang, Wei
experimental part, p. 1977 - 1982 (2011/04/22)
An unexpected one-pot tandem procedure of 2-bromo-4,5-diazafluoren-9-one starting from phenanthroline with a yield of up to 50% has been described. The conversion mechanism involves three consecutive oxidation, bromination, and rearrangement reactions. A series of its hammer-shaped donor-acceptor organic semiconductors with solvent-dependent fluorescence have also been constructed via Ullman and/or Friedel-Crafts reaction. Diazafluorenes (DAFs) and derivatives are regarded as promising building blocks or candidates for donor-acceptor organic semiconductors.
