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

• 1121545-25-2 C₂₉H₂₀O 
• 181135-36-4 (8-phenylnaphthalene-1-yl)boronic acid 
• 206-44-0 fluoranthene 

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.

Compound and application thereof

The invention relates to a compound and application thereof. The compound has a structure as shown in a formula I. By introducing a carbazole structure of cycloheptatriene, the planarity of molecules is improved, and the transmission barrier of current carriers is reduced, so that an organic electroluminescent device comprising the compound has the advantages of low voltage and high efficiency.

Axially Chiral Stable Radicals: Resolution and Characterization of Blatter Radical Atropisomers

Atropisomers of three Blatter radicals were obtained by the addition of 8-substituted 1-naphthyllithiums to 3-phenyl and 3-t-butylbenzo[e][1,2,4]triazine and separated by chiral high-performance liquid chromatography. Their absolute configurations were assigned by a comparison of experimental and time-dependent density functional theory calculated electronic circular dichroism spectra. The free energy of activation, ΔG?298, and the half life of racemization, t1/2, at 298 K were determined at ～25 kcal mol-1 and 130 h, respectively. Intramolecular π-πinteractions in radicals were evident from single-crystal X-ray diffraction, density functional theory, and electrochemical analyses.