861242-82-2 Usage
General Description
3-bromo-1,10-phenanthroline-5,6-dione is a chemical compound that belongs to the class of phenanthroline derivatives. It is a yellow to orange crystalline solid with the molecular formula C12H6BrN2O2. 3-bromo-1,10-phenanthroline-5,6-dione is used in various applications, including coordination chemistry, organic synthesis, and chemical analysis. It has been studied for its potential antitumor and antibacterial properties. Additionally, 3-bromo-1,10-phenanthroline-5,6-dione is known to exhibit fluorescent properties, making it useful for fluorescent labeling and imaging studies. Overall, this compound has a range of potential applications in research and industry due to its unique chemical and physical properties.
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.
