59951-65-4

Basic information

• Product Name: 1-Bromo-4-phenylnaphthalene
• Synonyms: 1-Bromo-4-phenylnaphthalene;Naphthalene, 1-bromo-4-phenyl-;1-Bromo-4-phenylphthalene;8-bromo-1-chlorodibenzo[b,d]furan;N-([1,1'-biphenyl]-4-yl)-4'-chloro-N-phenyl-[1,1'-biphenyl]-4-amine
• CAS NO: 59951-65-4
• Molecular Formula: C₁₆H₁₁Br
• Molecular Weight: 283.16254
• Mol File: 59951-65-4.mol
• Article Data: 16

Chemical Properties

• Melting Point: 76-77℃
• Boiling Point: 153°C/1mmHg(lit.)
• Appearance: /
• Density: 1.381±0.06 g/cm3 (20 ºC 760 Torr)
• Solubility: soluble in Toluene
• CAS DataBase Reference: 1-Bromo-4-phenylnaphthalene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Bromo-4-phenylnaphthalene(59951-65-4)
• EPA Substance Registry System: 1-Bromo-4-phenylnaphthalene(59951-65-4)

Safety Data

• Hazardous Substances Data: 59951-65-4(Hazardous Substances Data)

Usage

General Description

1-Bromo-4-phenylnaphthalene is a chemical compound that belongs to the class of organic compounds known as naphthalenes. It is a white to off-white crystalline powder that is sparingly soluble in water. 1-Bromo-4-phenylnaphthalene is primarily used in the synthesis of various organic compounds and can also be used as a building block in the production of pharmaceuticals, agrochemicals, dyes, and other fine chemicals. It is also used as a reagent in organic synthesis and as an intermediate in the production of specialty chemicals. Additionally, 1-Bromo-4-phenylnaphthalene is considered to have potential mutagenic and irritant properties, and as such, caution should be exercised when handling and using this compound.

Upstream product

• 75-15-0 carbon disulfide 
• 605-02-7 1-phenylnaphthalene 
• 7726-95-6 bromine 
• 63279-58-3 1-iodo-4-bromo-naphthalene 
• 98-80-6 phenylboronic acid 
• 83-53-4 1,4-dibromonaphthalene 
• 145965-14-6 1-bromo-4-(dihydroxyboryl)naphthalene 
• 591-50-4 iodobenzene 
• 90-11-9 1-Bromonaphthalene 
• 108-86-1 bromobenzene 
• 529-34-0 3,4-dihydronaphthalene-1(2H)-one 
• 7469-40-1 1-phenyl-3,4-dihydronaphthalene 

Downstream Products

• 1674-21-1 Diphenyl-<4-phenyl-naphthyl-(1)>-carbinol 
• 1674-20-0 Diphenyl-(4-phenyl-naphthyl-⁽¹⁾)-chlormethan 
• 94574-45-5 4-phenyl-1-naphthoic acid 
• 949462-13-9 C₅₆H₄₀N₂ 
• 1422181-39-2 1-[1-(4-phenylnaphthalen-1-yl)naphthalen-2-yl]ethanone 
• 1422181-41-6 C₈₄H₅₄ 
• 1422181-38-1 4,4,5,5-tetramethyl-2-(4-phenylnaphthalen-1-yl)-1,3,2-dioxaborolane 

Relevant articles and documents

Synthesis and properties of chromophore-functionalized monovinylsilsesquioxane derivatives

A facile and efficient Pd-based Suzuki-Miyaura coupling reaction leading to mixed chromophores with styryl fragments, enabling their further application, is presented. We also disclose their use in the formation of monofunctionalized silsesquioxanes with a chromophore group covalently bound to a T8 core that have been prepared via a cross-metathesis reaction. These new materials were studied in terms of their photophysical and also thermal properties.

NOVEL COMPOUND AND ORGANIC ELECTROLUMINESCENT DEVICE COMPRISING THE SAME

Organic electroluminescent devices with lowered driving voltages, and enhanced efficiencies and lifetimes are provided.

Annular N-heterocycle double-carbene palladium coordination compound and preparation method and application thereof

The invention discloses an annular N-heterocycle double-carbene palladium coordination compound and a preparation method and application thereof. 1,4-2(N-ethyl-benzimidazole onium methyl)-2,3,5,6-tetramethylbenzene arene salt is used as a precursor of the annular N-heterocycle double-carbene palladium coordination compound. The synthetic annular N-heterocycle double-carbene palladium coordinationcompound is used as a catalyst and used for catalyzing the cross-coupling reaction of carbon-carbon bonds. The preparation method of the annular N-heterocycle double-carbene palladium coordination compound comprises the steps that under nitrogen protection, 1,4-2(N-ethyl-benzimidazole onium methyl)-2,3,5,6-tetramethylbenzene arene salt and metal compounds are added to a reaction vessel according to a molar ratio of 1:(2-5), an organic solvent is added to the mixture, then reaction is conducted for 12-24 hours under the temperature of 0-100 DEG C, the mixture is filtered and subjected to etherdiffusion, and the annular N-heterocycle double-carbene palladium coordination compound is obtained. The prepared annular N-heterocycle double-carbene palladium coordination compound is mainly appliedto the technical field of catalysts.