54523-47-6

Basic information

• Product Name: 1,3-Bis(4-bromophenyl)propanone
• Synonyms: 1,3-bis(4-bromophenyl)propanone;4,4'-Dibromodibenzyl ketone;1,3-Bis(4-bromophenyl)-2-propanone;1,3-Bis(4-bromophenyl)acetone;1,3-Bis(4-bromopheny;1,3-. Molecular ForMula;1,3-Bis(4-broMophenyl)propan-1-one;1,3-Bis(4-bromophenyl)
• CAS NO: 54523-47-6
• Molecular Formula: C₁₅H₁₂Br₂O
• Molecular Weight: 368.06
• Product Categories: Naphthyridine,Quinoline
• Mol File: 54523-47-6.mol
• Article Data: 40

Chemical Properties

• Melting Point: 117.0 to 121.0 °C
• Boiling Point: 427 °C
• Flash Point: 114 °C
• Appearance: /
• Density: 1.607
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.619
• CAS DataBase Reference: 1,3-Bis(4-bromophenyl)propanone(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Bis(4-bromophenyl)propanone(54523-47-6)
• EPA Substance Registry System: 1,3-Bis(4-bromophenyl)propanone(54523-47-6)

Safety Data

• Hazardous Substances Data: 54523-47-6(Hazardous Substances Data)

Usage

Chemical Properties

off-white powder

InChI:InChI=1/C15H12Br2O/c16-13-5-1-11(2-6-13)9-15(18)10-12-3-7-14(17)8-4-12/h1-8H,9-10H2

Upstream product

• 14062-25-0 Ethyl 4-bromophenylacetate 
• 41841-16-1 (4-bromo-phenyl)-acetic acid methyl ester 
• 4755-77-5 Ethyl oxalyl chloride 
• 589-15-1 1-bromomethyl-4-bromobenzene 
• 201230-82-2 carbon monoxide 
• 1878-68-8 2-(4-bromophenyl)-acetic acid 
• 38622-91-2 [(p-methylphenyl)sulfonylmethyl]isonitrile 
• 13463-40-6 iron pentacarbonyl 
• 37859-24-8 2-(4-bromophenyl)acetyl chloride 
• 541-41-3 chloroformic acid ethyl ester 
• 589-17-3 p-bromobenzyl chloride 

Downstream Products

• 23923-22-0 2,3,5-tris(4-bromophenyl)-4-phenylcyclopenta-2,4-dienone 
• 4939-72-4 p-bromobenzyl radical 
• 105457-21-4 C₈H₆BrO 
• 131273-92-2 1,3-bis(4-bromophenyl)cyclopentaphenanthren-2-one 
• 158230-09-2 [2-(4-Bromo-benzyl)-3-(4-bromo-phenyl)-2-hydroxy-propyl]-(2,4,6-triisopropyl-phenyl)-phosphinic acid methyl ester 
• 54523-26-1 C₅₂H₃₀Br₄O₂ 
• 38267-83-3 2,5-Bis-(4-bromo-phenyl)-3,4-bis-(3-iodo-phenyl)-cyclopenta-2,4-dienone 
• 38267-82-2 2,5-Bis-(4-bromo-phenyl)-3,4-bis-(3-bromo-phenyl)-cyclopenta-2,4-dienone 
• 38268-28-9 2,5-Bis-(4-bromo-phenyl)-3,4-bis-(3-chloro-phenyl)-cyclopenta-2,4-dienone 
• 325834-46-6 1,3-bis(4-((triisopropylsilyl)ethynyl)phenyl)propan-2-one 
• 327603-95-2 2,5-bis(4-bromophenyl)-3,4-di(4-dodecylphenyl)cyclopenta-2,4-dien-1-one 
• 347390-22-1 1,3-bis(4-(3,7-dimethyloctanyl)phenyl)-2-propanone 
• 347390-18-5 1,3-bis(4-bromophenyl)-2-propanone ethylene acetal 
• 493015-32-0 3,3,9,9-tetrakis[(4-bromophenyl)methyl]-2,4,8,10-tetraoxaspiro[5.5]undecane 

Relevant articles and documents

Synthesis, Photophysical and Supramolecular Properties of a π-Conjugated Molecular Crown Containing a Pentagonal Unit: A Model Compound for Fullerene C 240

The total synthesis of carbon onions is a significant challenge in the fields of materials science and organic chemistry. To date, the synthesis of even a fragment of fullerene C 240and its smallest carbon onion C 60?C 240remains poorly explored. Herein, we demonstrate a bottom-up strategy to produce a novel π-extended molecular crown-shaped molecule (MC3) containing curved pentagonal and hexagonal units. This molecular crown represents a curved model compound for fullerene C 240and is fully characterized by NMR, mass spectrometry, UV-vis absorption, and from its emission spectra. Its supramolecular host-guest interaction with fullerene C 60is also investigated. MC3 and C 60?MC3 can potentially be employed as seeds or templates for the bottom-up synthesis of fullerene C 240and the carbon onion C 60?C 240, respectively.

Catalytic Asymmetric (3 + 3) Cycloaddition of Oxyallyl Zwitterions with α-Diazomethylphosphonates

The unique structure of oxyallyls represents a significant challenge for their catalytic asymmetric applications. Herein, an unprecedented chiral imidodiphosphoric acid-catalytic enantioselective (3 + 3) cycloaddition between oxyallyl zwitterions generate

Triphenylene-Enchained Perfluorocyclobutyl Aryl Ether Polymers: A Modular Synthetic Route to Processable Thermoplastics Approaching Upper Limit Tgand Photostability

Triphenylene-containing trifluorovinyl ether monomers prepared from 2,3-disubstituted-bis-1,4-(p-bromophenyl)triphenylene core building blocks undergo thermal step-growth polymerization (Ph2O, 180 °C), affording perfluorocyclobutyl polymers with unprecede