98905-03-4

Basic information

• Product Name: 3-bromo-1,1′: 3′1″-terphenyl
• Synonyms: 3-bromo-1,1′: 3′1″-terphenyl
• CAS NO: 98905-03-4
• Molecular Weight: 309.205
• Mol File: 98905-03-4.mol

Chemical Properties

• Boiling Point: 413.1±14.0 °C(Predicted)
• Density: 1.309±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 3-bromo-1,1′: 3′1″-terphenyl(CAS DataBase Reference)
• NIST Chemistry Reference: 3-bromo-1,1′: 3′1″-terphenyl(98905-03-4)
• EPA Substance Registry System: 3-bromo-1,1′: 3′1″-terphenyl(98905-03-4)

Safety Data

• Hazardous Substances Data: 98905-03-4(Hazardous Substances Data)

Upstream product

• 591-18-4 1-Bromo-3-iodobenzene 
• 5122-95-2 3-Biphenylboronic acid 
• 16400-51-4 3,3'-dibromobiphenyl 
• 98-80-6 phenylboronic acid 
• 912844-88-3 2-([1,1’-biphenyl]-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 2113-57-7 3-bromobiphenyl 
• 92960-08-2 3-(3-bromophenyl)cyclohex-2-enone 

Downstream Products

• 83777-43-9 2-(3-biphenilyl)-m-quaterphenyl 
• 934603-99-3 B-[1,1′:3′,1″-terphenyl]-3-ylboronic acid 
• 1293372-84-5 4,4'-(1-phenylethane-1,1-diyl)bis(N,N-bis(3-(biphenyl-3-yl)phenyl)aniline) 
• 1293372-83-4 4,4'-(diphenylmethylene)bis(N,N-bis(3-(biphenyl-3-yl)phenyl)aniline) 
• 1402225-90-4 C₃₃H₂₂ClN₃ 
• 1115023-84-1 2-([1,1‘:3’,1“-terphenyl]-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 

Relevant articles and documents

Adamantane-containing compound, high polymer, mixture, composition, and electronic device

The invention discloses an adamantane-containing compound represented by general formula (1), and a high polymer, a mixture, a composition and an electronic device containing the same. Adamantane andan electron-deficient unit are connected to serve as a core unit, and then are matched with other functional units in order to effectively increase the intermolecular distance and reduce the intermolecular interaction, so the effects of reducing exciton quenching and improving the energy utilization rate are achieved, and the performances of the compound and the related device are further improved.

Organic electroluminescent compounds, organic electroluminescent devices and applications thereof

The invention relates to the field of light-emitting materials and particularly provides an organic electroluminescence compound, an organic electroluminescence device and application thereof. The structural formula of the organic electroluminescence compound is as shown below in the description. The compound can serve as an HTL, EBL, B-dopant, Host, EBL, ETL and CPL material. When used in the organic electroluminescence device, the organic electroluminescence compound can reduce driving voltage and improve luminous efficiency, brightness, heat stability, color purity and the service life of the device.

POLYCYCLIC AROMATIC COMPOUND AND LIGHT EMISSION LAYER-FORMING COMPOSITION

The objective of the invention is to provide a polycyclic aromatic compound in which solubility to a solvent, film formability, wet coatability, thermal stability, and in-plane orientation are improved. This objective is achieved by a light emission layer

ORGANIC OPTOELECTRONIC DEVICE AND DISPLAY APPARATUS

The present invention relates to an organic optoelectronic device and a display apparatus comprising same, the organic optoelectronic device comprising: an anode and a cathode facing each other; a light-emitting layer located between the anode and cathode; a hole transport layer located between the anode and light-emitting layer; an auxiliary hole transport layer located between the hole transport layer and light-emitting layer; an electron transport layer located between the cathode and light-emitting layer; and an auxiliary electron transport layer between the electron transport layer and light-emitting layer, wherein the auxiliary electron transport layer comprises at least one type of a first compound expressed by a particular Chemical Formula, and the auxiliary hole transport layer comprises at least one type of a second compound expressed by a particular Chemical Formula.

Synthetic method of directly coupling aryl halide by aromatic hydrocarbon Grignard reagent in the presence of recycled modified palladium-charcoal

The invention provides a synthetic method of directly coupling aryl halide by an aromatic hydrocarbon Grignard reagent. The synthetic method includes performing reflux and water separation of a catalyst Pd/C and an azeotropic organic solvent of non-halogenated hydrocarbon and water, adding an organic phosphine ligand, performing a complexation reaction to obtain a catalyst organic phosphine ligand complexing Pd/C, using aryl halide as an initial material, performing a Grignard reaction at 10-90 DEG C to obtain a Grignard reagent, adding the catalyst, performing a coupled reaction of aryl halide and the Grignard reagent to obtain a coupling aromatic hydrocarbon. The synthetic method uses one-step method, has low synthesis cost, is green and environmental friendly, and is a high-efficiency and clean synthetic technology of coupling aryl halide.

COMPOSITION FOR ORGANIC OPTOELECTRIC DEVICE AND ORGANIC OPTOELECTRIC DEVICE AND DISPLAY DEVICE

The present invention relates to: a composition for an organic photoelectric device, which comprises a first host compound represented by the chemical formula I and a second host compound represented by the chemical formula II; an organic photoelectric device including the composition for an organic photoelectric device; and a display device. In the chemical formula I and II, Z, R^1 to R^3, L^1 to L^3, R^4 to R^19, and n are the same as defined in the specification.COPYRIGHT KIPO 2016

COMPOUND, ORGANIC OPTOELECTRIC DEVICE AND DISPLAY DEVICE

The present invention relates to: a compound represented by chemical formula 1; an organic optoelectronic diode containing the same; and a display device containing the organic optoelectronic diode. The description of chemical formula 1 is the same as that which was defined in the specification.

ANTHRACENE DERIVATIVE AND ORGANIC ELECTROLUMINESCENT ELEMENT USING THE SAME

PROBLEM TO BE SOLVED: To provide an anthracene derivative desirably having controlled solubility, deposition property, wet coating property and orientation property (further desirably thermal stability) and an electroluminescent element excellent in at least one of efficacy, life and driving voltage by using the compound as a constituent of the electroluminescent element. SOLUTION: There is provided an anthracene derivative represented by the following formula (1). Ar-An-L-FG (1), where An is anthracene, Ar is aryl having 6 to 18 carbon atoms which may be substituted, L is arylene having 7 to 18 carbon atoms which may be substituted and 2 or more rings are condensed and FG is an oligophenylene structure bound at a meta position which may be substituted (functional group). SELECTED DRAWING: None COPYRIGHT: (C)2016,JPOandINPIT

ORGANIC COMPOUND AND COMPOSITION AND ORGANIC OPTOELECTRIC DEVICE AND DISPLAY DEVICE

The present invention relates to: an organic compound represented by chemical formula 1; a composition for an organic electroluminescent device comprising the organic compound; an organic electroluminescent device that employs the organic compound or the composition; and a display device comprising the organic electroluminescent device. In the chemical formula 1, Z, R1 to R3 and Ar1 are as defined in the specification.COPYRIGHT KIPO 2016

Organic compound and composition and organic optoelectric device and display device

Disclosed are an organic compound represented by the following Chemical Formula 1, a composition for an organic optoelectric device including the organic compound, an organic optoelectric device including the organic compound or the composition, and a display device including the organic optoelectric device. In the Chemical Formula 1, X, L1 to L6, R1 to R22, and n1 to n4 are the same as described in the detailed description.