1121545-24-1

Basic information

• Product Name: 1-Bromo-8-phenylnaphthalene
• Synonyms: 1-Bromo-8-phenylnaphthalene
• CAS NO: 1121545-24-1
• Molecular Formula: C₁₆H₁₁Br
• Molecular Weight: 283.16254
• Mol File: 1121545-24-1.mol
• Article Data: 20

Chemical Properties

• Boiling Point: 385.8±11.0 °C(Predicted)
• Appearance: /
• Density: 1.381±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 1-Bromo-8-phenylnaphthalene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Bromo-8-phenylnaphthalene(1121545-24-1)
• EPA Substance Registry System: 1-Bromo-8-phenylnaphthalene(1121545-24-1)

Safety Data

• Hazardous Substances Data: 1121545-24-1(Hazardous Substances Data)

Usage

General Description

1-Bromo-8-phenylnaphthalene, also known as 8-Bromonaphthylbenzene, is a chemical compound with the molecular formula C16H11Br. It is a white to off-white crystalline solid, commonly used in organic synthesis and as a building block for the production of various pharmaceuticals, including antitumor agents and HIV protease inhibitors. 1-Bromo-8-phenylnaphthalene can also be utilized as a reactant in the synthesis of other organic compounds and as a research reagent in chemical and pharmaceutical laboratories. Additionally, 1-Bromo-8-phenylnaphthalene may also have potential applications in materials science and in the development of new functional materials due to its unique chemical structure and properties.

Upstream product

• 17135-74-9 1,8-dibromonaphthalene 
• 24388-23-6 2-phenyl-4,4,5,5-tetramethyl-1,3,2-dioxoborole 
• 98-80-6 phenylboronic acid 

Downstream Products

• 181135-36-4 (8-phenylnaphthalene-1-yl)boronic acid 

Relevant articles and documents

Azabora[5]helicene Charge-Transfer Dyes Show Efficient and Spectrally Variable Circularly Polarized Luminescence

Three helicenes based on a borylated arylisoquinoline skeleton have been prepared in their enantiopure forms and characterized with respect to their photophysical properties, including the use of chiroptical spectroscopies. The dyes show varying charge-tr

ORGANIC ELECTROLUMINESCENT COMPOUND AND ORGANIC ELECTROLUMINESCENT DEVICE COMPRISING THE SAME

The present disclosure relates to an organic electroluminescent compound and an organic electroluminescent device comprising the same. By comprising the organic electroluminescent compound according to the present disclosure, it is possible to provide an organic electroluminescent device having good thermal stability, low driving voltage, high luminous efficiency and/or improved lifetime properties.

Asymmetric Catalytic Approach to Multilayer 3D Chirality

The first asymmetric catalytic approach to multilayer 3D chirality has been achieved by using Suzuki-Miyaura cross-couplings. New chiral catalysts were designed and screened under various catalytic systems that proved chiral amide-phosphines to be more efficient ligands than other candidates. The multilayer 3D framework was unambiguously determined by X-ray structural analysis showing a parallel pattern of three layers consisting of top, middle and bottom aromatic rings. The X-ray structure of a catalyst complex, dichloride complex of Pd-phosphine amide, was obtained revealing an interesting asymmetric environment nearby the Pd metal center. Three rings of multilayer 3D products can be readily changed by varying aromatic ring-anchored starting materials. The resulting multilayer products displayed strong luminescence under UV irradiation and strong aggregation-induced emission (AIE). In the future, this work would benefit not only the field of asymmetric synthesis but also materials science, in particular polarized organic electronics, optoelectronics and photovoltaics.

Compound and application thereof

The invention relates to a compound and application thereof. The compound has a structure represented by formula I shown in the specification. The compound provided by the invention takes a 7-membered conjugated aromatic ring as a parent nucleus structure, a substituent group must contain one carbazole and a derivative group (Ar) thereof, carbazole ensures a corresponding HOMO energy level and provides good hole capability, and the addition of the 7-membered aromatic ring provides a larger planar conjugated group, so that the carrier mobility of the whole molecule is increased, and the hole mobility is improved. Moreover, due to the introduction of the rigid structure, the material has high glass transition temperature and excellent thermal stability, can effectively improve the device efficiency and reduce the driving voltage when being applied to OLED devices, and is especially a good hole-type main body material.