6864-20-6 Usage
Description
2,4,6-Triphenylaniline is an organic compound that consists of an aniline molecule with three phenyl groups attached to the 2nd, 4th, and 6th positions. It is known for its ability to be oxidized to azo(2,4,6-triphenylbenzene) in acetonitrile containing pyridine. This characteristic makes it a potentially useful compound in various applications.
Uses
Used in Chemical Synthesis:
2,4,6-Triphenylaniline is used as a starting material for the synthesis of various organic compounds, particularly those involving the formation of azo dyes and other related structures. Its unique structure allows for the creation of a wide range of derivatives with diverse properties and applications.
Used in Dye Manufacturing:
2,4,6-Triphenylaniline is used as a precursor in the production of azo dyes, which are widely used in the textile, plastics, and printing industries. The oxidation of 2,4,6-triphenylaniline to azo(2,4,6-triphenylbenzene) enables the creation of dyes with specific color properties and stability.
Used in Research and Development:
2,4,6-Triphenylaniline serves as a valuable compound for research purposes, particularly in the fields of organic chemistry and materials science. Its reactivity and structural properties make it an interesting subject for studying various chemical reactions and exploring new applications.
Used in Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, 2,4,6-triphenylaniline could potentially be used in the pharmaceutical industry as a building block for the development of new drugs or drug candidates. Its structural diversity and reactivity may allow for the creation of compounds with specific biological activities or properties.
Check Digit Verification of cas no
The CAS Registry Mumber 6864-20-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,6 and 4 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6864-20:
(6*6)+(5*8)+(4*6)+(3*4)+(2*2)+(1*0)=116
116 % 10 = 6
So 6864-20-6 is a valid CAS Registry Number.
InChI:InChI=1/C24H19N/c25-24-22(19-12-6-2-7-13-19)16-21(18-10-4-1-5-11-18)17-23(24)20-14-8-3-9-15-20/h1-17H,25H2
6864-20-6Relevant articles and documents
NOVEL COMPOUND AND ORGANIC ELECTROLUMINESCENT DIVICE INCLUDING THE SAME
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Paragraph 0128; 0132-0136, (2019/03/30)
The present invention relates to a novel arylamine compound, which facilitates hole injection and hole transport, thereby exhibiting effects of low voltage and low power consumption. In addition, the novel arlyamine compound exhibits high efficiency by having high LUMO, which enables electronic blocking, due to a wide band gap and can increase thermal stability through Tg rise by increasing robustness in a molecule, thereby stabilizing the life of a device.COPYRIGHT KIPO 2019
Facile synthesis of mono-, bis- and tris-aryl-substituted aniline derivatives in aqueous DMF
Liu, Chun,Song, Xiaoxiao,Ni, Qijian,Qiu, Jieshan
, p. 62 - 75,14 (2020/09/02)
A facile, efficient and general protocol for synthesizing a series of mono-, bis- and tris-arylsubstituted aniline derivatives is described via the Pd(OAc)2-catalyzed aerobic and ligand-free Suzuki reaction of mono-, di- and tribromoanilines with aryl boronic acids in aqueous N,Ndimethylformamide (DMF). This is the first example to prepare 2,6-bisaryl-4-nitroanilines and 2,6-bisarylanilines via a palladium-catalyzed ligand-free Suzuki reaction.
Enantioselective organocatalytic Biginelli reaction: Dependence of the catalyst on sterics, hydrogen bonding, and reinforced chirality
Saha, Satyajit,Moorthy, Jarugu Narasimha
supporting information; experimental part, p. 396 - 402 (2011/04/17)
From a systematic investigation involving the synthesis of a series of catalysts and screening studies, the organocatalyst 16, which is sterically hindered, contains a strong hydrogen-bonding site, and is endowed with reinforced chirality, is shown to pro