274905-73-6

Basic information

• Product Name: 2-TERTBUTYL-9,10-DI(2-NAPHTHYL)ANTHRACENE
• Synonyms: 2-TERTBUTYL-9,10-DI(2-NAPHTHYL)ANTHRACENE;2-tert-butyl-9,10-di(naphth-2-yl)anthracene;3-tert-Butyl-9,10-di(naphth-2-yl)anthracene;TBADN , 2-Methyl-9,10-bis(naphthalen-2-yl)anthracene;2-tert-butyl-9,10-di(naphthalen-3-yl)anthracene;2-tert-butyl-9,10-bis(naphthalen-2-yl)anthracene;2-tert-butyl-9,10-dinaphthalen-2-ylanthracene;2-Tert-butyl-9,10-bis (2-naphthyl) anthracene
• CAS NO: 274905-73-6
• Molecular Formula: C38H30
• Molecular Weight: 486.64
• Product Categories: Electronic Chemicals;oled materials
• Mol File: 274905-73-6.mol

Chemical Properties

• Boiling Point: 624.807 °C at 760 mmHg
• Flash Point: 335.625 °C
• Appearance: /
• Density: 1.15 g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.709
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 2-TERTBUTYL-9,10-DI(2-NAPHTHYL)ANTHRACENE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-TERTBUTYL-9,10-DI(2-NAPHTHYL)ANTHRACENE(274905-73-6)
• EPA Substance Registry System: 2-TERTBUTYL-9,10-DI(2-NAPHTHYL)ANTHRACENE(274905-73-6)

Safety Data

• Statements: 53
• Hazardous Substances Data: 274905-73-6(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
2-TERTBUTYL-9,10-DI(2-NAPHTHYL)ANTHRACENE is used as a key intermediate in organic synthesis for the development of new functional materials and compounds with specific properties.
Used in Materials Science:
In the field of materials science, 2-TERTBUTYL-9,10-DI(2-NAPHTHYL)ANTHRACENE is used as a building block for the synthesis of advanced materials with unique properties, such as improved stability and solubility.
Used in Organic Electronics:
2-TERTBUTYL-9,10-DI(2-NAPHTHYL)ANTHRACENE is used as a component in the development of organic light-emitting diodes (OLEDs) and photovoltaic devices, owing to its potential application in enhancing the performance and efficiency of these devices.
Used in Optoelectronic Devices:
In the optoelectronic industry, 2-TERTBUTYL-9,10-DI(2-NAPHTHYL)ANTHRACENE is utilized for its photophysical properties, making it a valuable compound in the design and fabrication of optoelectronic devices with improved performance and functionality.

InChI:InChI=1/C38H30/c1-38(2,3)31-20-21-34-35(24-31)37(30-19-17-26-11-5-7-13-28(26)23-30)33-15-9-8-14-32(33)36(34)29-18-16-25-10-4-6-12-27(25)22-29/h4-24H,1-3H3

Upstream product

• 18801-00-8 2-(t-butyl)anthracene 
• 32316-92-0 naphthalene-2-boronic acid 
• 114583-08-3 2-tert-butyl-9,10-dibromoanthracene 
• 580-13-2 2-bromonaphthalene 
• 920979-25-5 C₃₈H₃₂O₂ 
• 474688-76-1 2-bromo-9,10-di(2-naphthyl)anthracene 
• 677-22-5 tert-butylmagnesium chloride 

Relevant articles and documents

Efficient blue organic light-emitting devices based on novel anthracence derivatives with pronounced thermal stability and excellent film-forming property

A series of anthracene based blue host materials was synthesized and characterized with respect to their chemical, luminescence, film-forming and thermal properties. The anthracene derivatives are strongly blue fluorescent (λf = 435-445 nm) with high fluorescence quantum yields (Φf = 0.71-0.85). All of these compounds have excellent film-forming properties and thermal properties. Organic light-emitting devices (OLEDs) fabricated using these three compounds as blue host emitter and using 0.5-wt% tetra (t-butyl) perylene (TBPe) dopant in the emitting layer exhibit good light emitting performance with bright blue emission.

Ligand-free nickel-catalyzed Kumada couplings of aryl bromides with tert-butyl Grignard reagents

A ligand-free nickel-catalyzed Kumada cross-coupling of aryl bromides and tert-butyl Grignard reagents led to the formation of a series of tert-butyl aryls in moderate to good yields, excellent tBu/iBu ratios, and good functional group compatibility. A radical coupling process is indicated and a mechanism with a Ni(I)-Ni(III) catalytic cycle is proposed.

Synthesis process

A process for preparing a substituted or unsubstituted 9,10-diarylanthracene including reacting an organometallic substituted or unsubstituted aryl compound with a substituted or unsubstituted anthraquinone to yield a substituted or unsubstituted diol; an

Synthesis process

A process for preparing a substituted or unsubstituted 9,10-diaryl anthracene including reacting a substituted or unsubstituted anthracene with a halogenating agent to yield a halogenated anthracene, and reacting the halogenated anthracene with an aryl bo

Oligonaphthalene derivatives, and light-emitting element and light-emitting device using oligonaphthalene derivatives

The present invention provides a novel material capable of realizing excellent color purity of blue, a light-emitting element and a light-emitting device using the novel material. The present invention provides an oligonaphthalene derivative represented by the formula (1). The oligonaphthalene derivatives of the present invention have an extremely large band gap, can emit light with extremely short wavelength, and can emit blue light with favorable color purity. In addition, a light-emitting element that can exhibit excellent color purity of blue can be obtained by applying this material to the light-emitting element or a light-emitting device; therefore the light-emitting element having superior color reproducibility can be provided.