96761-85-2

Basic information

• Product Name: 1,3,5-Tris(3-bromophenyl)benzene
• Synonyms: 1,3,5-TRIS(3-BROMOPHENYL)BENZENE;1,3,5-tri-(3-bromophenyl)benzene;3,3''-Dibromo-5'-(3-bromophenyl)-1,1':3',1''-terphenyl;96761-85-2 cas;cas 96761-85-2;cas no 96761-85-2
• CAS NO: 96761-85-2
• Molecular Formula: C₂₄H₁₅Br₃
• Molecular Weight: 543.09
• EINECS: 1312995-182-4
• Mol File: 96761-85-2.mol
• Article Data: 13

Chemical Properties

• Melting Point: 170.0 to 174.0 °C
• Boiling Point: 553.9 °C at 760 mmHg
• Flash Point: 277.1 °C
• Appearance: /
• Density: 1.626 g/cm³
• Vapor Pressure: 9.57E-12mmHg at 25°C
• Refractive Index: 1.659
• Storage Temp.: Sealed in dry,Room Temperature
• Solubility: soluble in Toluene
• CAS DataBase Reference: 1,3,5-Tris(3-bromophenyl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,5-Tris(3-bromophenyl)benzene(96761-85-2)
• EPA Substance Registry System: 1,3,5-Tris(3-bromophenyl)benzene(96761-85-2)

Safety Data

• Hazardous Substances Data: 96761-85-2(Hazardous Substances Data)

Usage

General Description

1,3,5-Tris(3-bromophenyl)benzene is a chemical compound made up of a benzene ring with three bromine-substituted phenyl groups attached at the 1, 3, and 5 positions. It is commonly used in organic synthesis and can be utilized as an intermediate for producing high-performance polymers and liquid crystals. 1,3,5-Tris(3-bromophenyl)benzene’s structure and properties make it useful in a variety of applications, including in the development of electronic materials, fluorescence sensors, and pharmaceuticals. Additionally, its aromatic nature and reactivity make it a valuable building block for creating complex organic molecules in laboratory settings. Overall, 1,3,5-Tris(3-bromophenyl)benzene has diverse potential applications in various industries due to its unique structural and chemical characteristics.

InChI:InChI=1/C24H15Br3/c25-22-7-1-4-16(13-22)19-10-20(17-5-2-8-23(26)14-17)12-21(11-19)18-6-3-9-24(27)15-18/h1-15H

Upstream product

• 766-81-4 3-bromophenylacetylene 
• 767-00-0 4-cyanophenol 
• 2142-63-4 1-(3-Bromophenyl)ethanone 
• 95-20-5 2-methyl-1H-indole 

Downstream Products

• 118688-54-3 3,3',3''-(1,3,5-Benzoltriyl)tris(benzoesaeure) 
• 1197989-90-4 C₂₉H₁₉Br₂N 
• 1165939-26-3 1,3-bis(3-pyridinephenyl)-5-(3-bromophenyl)benzene 
• 1206531-96-5 C₄₅H₃₆O₃ 
• 1395348-23-8 C₄₂H₃₀O₃ 
• 1395348-25-0 C₅₁H₃₆O₃ 
• 1311378-95-6 (5'-(3-(diphenylphosphoryl)phenyl)[1,1':3',1''-terphenyl]-3,3''-diyl)bis(diphenylphosphine oxide) 
• 196505-74-5 C₄₈H₃₀ 

Relevant articles and documents

Extended phenylene based microporous organic polymers with selective carbon dioxide adsorption

Two microporous conjugated polymers with extended phenylene backbones have been synthesized through Suzuki cross-coupling reactions. The structure and the pores of the polymers have been controlled by the use of para- and meta-structure directing 1,3,5-triphenyl tribromide monomers. Gas sorption studies revealed an unprecedented CO2 selectivity over N2 for these conjugated polymer networks. The networks have furthermore been tested as hydrogen storage materials and showed significant hydrogen uptake at high pressures.

Solvent-dependent metal-free chemoselective synthesis of benzimidazoles and 1,3,5-triarylbenzenes from 2-amino anilines and aryl alkyl ketones catalyzed by I2

A solvent-dependent I2-catalyzed chemoselective reaction was developed for the synthesis of benzimidazoles and 1,3,5-triarylbenzenes via the annulation of 2-amino anilines and aryl alkyl ketones or the cyclization of aryl alkyl ketones, respectively. With 1,4-dioxane as the solvent, sequential C[sbnd]N bond formation followed by C(CO)-C(CH3) bond cleavage leads to the formation of benzimidazoles in a highly selective manner while aldol-type self-condensation of aryl alkyl ketones predominates using PhNO2 or PhCl as the solvent to afford 1,3,5-triarylbenzenes.

DBSA catalyzed cyclotrimerization of acetophenones: An efficient synthesis of 1,3,5-triarylbenzenes under solvent-free conditions

A facile method for the synthesis of 1,3,5-triarylbenzenes is developed via cyclotrimerization of acetophenones in the presence of 4-dodecylbenzenesulfonic acid (DBSA) as an efficient Bronsted acid catalyst under solvent-free conditions. This synthetic pr