374592-88-8 Usage
General Description
N4,N4'-Di-1-naphthalenyl-N4,N4'-di-2-naphthalenyl-[1,1'-biphenyl]-4,4'-diamine, also known as 2,2',6,6'-tetra(1-naphthyl)-4,4'-diaminobiphenyl (TNDB), is a chemical compound consisting of two 1-naphthyl and two 2-naphthyl groups linked to a biphenyl core, with diamine groups at the 4,4' positions. N4,N4'-Di-1-naphthalenyl-N4,N4'-di-2-naphthalenyl-[1,1'-biphenyl]-4,4'-diamine is commonly used as a charge transport material in organic electroluminescent devices and as a hole injection layer in organic light-emitting diodes. TNDB exhibits high thermal stability, good hole transport properties, and a low ionization potential, making it a useful material for improving the efficiency and stability of organic electronic devices. Additionally, it has potential applications in organic photovoltaic cells and organic thin-film transistors due to its favorable electronic and optical properties.
Check Digit Verification of cas no
The CAS Registry Mumber 374592-88-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,7,4,5,9 and 2 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 374592-88:
(8*3)+(7*7)+(6*4)+(5*5)+(4*9)+(3*2)+(2*8)+(1*8)=188
188 % 10 = 8
So 374592-88-8 is a valid CAS Registry Number.
374592-88-8Relevant articles and documents
PROCESS FOR FORMING AN AROMATIC AMINE COMPOUND
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Page/Page column 15-16, (2008/06/13)
A process for forming an aromatic amine product comprises the steps of (a) combining an aromatic primary or secondary initial amine with an aromatic halide compound in the presence of a palladium complex and a phosphine compound catalyst to form a mixture; (b) heating the mixture to a first temperature of at least 60°C; (c) adding a base material to the heated mixture; and (d) maintaining the temperature of the mixture at or above the first temperature for a period of time sufficient to form as a product an aromatic substituted form of the aromatic primary or secondary initial amine. The process provides products of high purity in good yields.