112752-09-7 Usage
Uses
Used in Organic Synthesis:
Phenol, 4-nitro-2-(2-quinolinyl)-, is used as a reagent in organic synthesis for its ability to participate in various chemical reactions, such as nucleophilic aromatic substitution, electrophilic aromatic substitution, and redox reactions. Its presence of both nitro and phenol groups allows for the formation of diverse products, making it a versatile building block in the synthesis of complex organic molecules.
Used in Pharmaceutical Research:
In the pharmaceutical industry, Phenol, 4-nitro-2-(2-quinolinyl)-, is used as a starting material or intermediate in the development of new drugs. Its unique structure and reactivity can be exploited to design and synthesize novel compounds with potential therapeutic properties. Phenol, 4-nitro-2-(2-quinolinyl)may also be used in the synthesis of active pharmaceutical ingredients (APIs) or as a key component in the formulation of drug delivery systems.
Used in Research and Laboratory Settings:
Phenol, 4-nitro-2-(2-quinolinyl)-, is used as a research tool in academic and industrial laboratories. Its unique chemical properties make it suitable for studying various aspects of organic chemistry, such as reaction mechanisms, stereochemistry, and the influence of functional groups on reactivity. Additionally, it can be used to explore the synthesis of new compounds with potential applications in various fields, including materials science, agrochemistry, and environmental chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 112752-09-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,7,5 and 2 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 112752-09:
(8*1)+(7*1)+(6*2)+(5*7)+(4*5)+(3*2)+(2*0)+(1*9)=97
97 % 10 = 7
So 112752-09-7 is a valid CAS Registry Number.
112752-09-7Relevant academic research and scientific papers
Synthesis, characterization and photoluminescence properties of strong fluorescent BF2 complexes bearing (2-quinolin-2-yl)phenol ligands
Ma, Ru-Zheng,Yao, Qi-Chao,Yang, Xi,Xia, Min
scheme or table, p. 93 - 98 (2012/05/19)
Novel N,O bidentate BF2 complexes were prepared in good to excellent yields through the coordination of (2-quinolin-2-yl)phenol and its derivatives with boron trifluoride etherate under mild conditions. These fluorine-boron complexes exhibited strong fluorescence both in organic solvents and in solid state. Their photophysical properties were thoroughly studied by absorption and fluorescence spectroscopy in various solvents. The electronic and site effects of substituents on phenolic and quinolinyl rings were found to have a profound impact on quantum yields. All these complexes were fully characterized by IR, 1H, 13C, 19F NMR and microanalysis. The high quantum yields and large Stokes shifts make these compounds as potential fluorescent dyes.
TAUTOMERS OF AZINE DERIVATIVES. 21. TAUTOMERISM IN 2-(2-HYDROXYARYL)AZINES
Stekhova, S. A.,Lapachev, V. V.,Mamaev, V. P.
, p. 65 - 70 (2007/10/02)
Tautomerism in 2-(2-hydroxyaryl)azines has been studied using 17O NMR and UV spectroscopy.Consideration has been given to the influence of solvent and structural factors which facilitate the establishment of a tautomeric equilibrium in these compounds.
