116341-90-3 Usage
Description
[2,2'-Bi-1H-indene]-1,1',3,3'(2H,2'H)-tetrone, 5,5'-dibromo-2,2'-bis[4-(dimethylamino)phenyl]is a complex organic compound featuring a tetrone ring system with two 2,2'-Bi-1H-indene groups and two 5,5'-dibromo-2,2'-bis[4-(dimethylamino)phenyl] substituents. The tetrone ring, also known as a quinone, contains four carbonyl groups and is often utilized as a building block in organic synthesis. [2,2'-Bi-1H-indene]-1,1',3,3'(2H,2'H)-tetrone,
5,5'-dibromo-2,2'-bis[4-(dimethylamino)phenyl]-'s structure, which includes bromine and dimethylamino groups, suggests potential applications in materials science, medicinal chemistry, and organic electronic devices. Its unique composition and functional groups make it a promising candidate for further research and application across various industries.
Uses
Used in Materials Science:
[2,2'-Bi-1H-indene]-1,1',3,3'(2H,2'H)-tetrone, 5,5'-dibromo-2,2'-bis[4-(dimethylamino)phenyl]is used as a building block for the development of novel materials due to its unique tetrone ring system and functional groups, which can contribute to the creation of advanced materials with specific properties.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, [2,2'-Bi-1H-indene]-1,1',3,3'(2H,2'H)-tetrone, 5,5'-dibromo-2,2'-bis[4-(dimethylamino)phenyl]can be employed as a starting point for the synthesis of new pharmaceutical compounds. Its structural features may allow for the development of drugs with specific targeting or therapeutic properties.
Used in Organic Electronic Devices:
[2,2'-Bi-1H-indene]-1,1',3,3'(2H,2'H)-tetrone,
5,5'-dibromo-2,2'-bis[4-(dimethylamino)phenyl]-'s tetrone ring system and functional groups also make it a potential candidate for use in the development of organic electronic devices, such as organic light-emitting diodes (OLEDs) or organic photovoltaics (OPVs), where its electronic properties can be harnessed for improved device performance.
Used in Chemical Research:
[2,2'-Bi-1H-indene]-1,1',3,3'(2H,2'H)-tetrone, 5,5'-dibromo-2,2'-bis[4-(dimethylamino)phenyl]serves as a valuable subject for chemical research, allowing scientists to explore its reactivity, stability, and potential applications in various chemical reactions and processes.
Check Digit Verification of cas no
The CAS Registry Mumber 116341-90-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,3,4 and 1 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 116341-90:
(8*1)+(7*1)+(6*6)+(5*3)+(4*4)+(3*1)+(2*9)+(1*0)=103
103 % 10 = 3
So 116341-90-3 is a valid CAS Registry Number.
116341-90-3Relevant articles and documents
INFLUENCE OF ONIUM SUBSTITUENT IN PHTHALOYL RING ON THERMODYNAMIC PARAMETERS OF EQUILIBRIUM BETWEEN DIMER AND FREE RADICALS OF 2-(4-DIMETHYLAMINOPHENYL)-1,3-INDANDIONES
Pisarenko, L. M.,Nikulin, V. I.,Blagorazumov, M. P.,Neiland, O. Ya.,Paulin'sh, L. L.
, p. 1379 - 1385 (2007/10/02)
2,2'-Bis diperchlorate and 2,2'-bis diperchlorate have very definite thermochromic and mechanochromic properties, owing to reversible dissociation into free radicals.The rupture energy of the central bond C2-C2' in 5-substituted 2,2'-bis in acetonitrile is 63-75 kJ/mole; in the dimer with the bulky 5-(2,4,6-triphenylpyridinium) substituent, the rupture energy is 51 kJ/mole.The equilibrium constants follow the Hammett equation (? = 1.53, acetonitrile, 293 K).Radicals with onium substituents are thermodynamically the most stable of the arylindandionyl radicals that are thus far known, owing to the significant contribution of electrostatic interactions.
THERMODYNAMIC PARAMETERS OF FREE RADICAL-DIMER EQUILIBRIA IN PHENYLINDANDIONE DERIVATIVES
Pisarenko, L. M.,Nikulin, V. I.,Gagarina, A. B.
, p. 1086 - 1091 (2007/10/02)
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DIECKMANN-SHAPIRO CONDENSATION OF SUBSTITUTED PHTHALIDES WITH p-DIMETHYLAMINOBENZALDEHYDE
Nikulin, V. I.,Pisarenko, L. M.
, p. 1680 - 1684 (2007/10/02)
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