852066-26-3

Basic information

• Product Name: 1,4-bis((2-bromophenyl)ethynyl)benzene
• Synonyms: 1,4-bis((2-bromophenyl)ethynyl)benzene
• CAS NO: 852066-26-3
• Molecular Weight: 436.145
• Mol File: 852066-26-3.mol

Chemical Properties

• CAS DataBase Reference: 1,4-bis((2-bromophenyl)ethynyl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-bis((2-bromophenyl)ethynyl)benzene(852066-26-3)
• EPA Substance Registry System: 1,4-bis((2-bromophenyl)ethynyl)benzene(852066-26-3)

Safety Data

• Hazardous Substances Data: 852066-26-3(Hazardous Substances Data)

Upstream product

• 38274-16-7 2-bromo-1-(trimethylsilylethynyl)benzene 
• 624-38-4 para-diiodobenzene 
• 766-46-1 2-bromo-1-ethynylbenzene 
• 583-55-1 1-Bromo-2-iodobenzene 
• 935-14-8 1,4-diethynylbenzene 

Downstream Products

• 1408317-39-4 1,4-bis(2(2-anilinylethynyl)phenylethynyl)benzene 
• 1399169-48-2 C₅₂H₄₈N₂O₂ 
• 1399169-54-0 C₄₆H₃₆N₂O₂ 
• 1399169-50-6 C₄₈H₄₀N₂O₂ 
• 1399169-46-0 C₅₂H₄₈N₂O₂ 
• 1399169-26-6 C₅₆H₄₀N₂O₂ 
• 1301743-14-5 C₆₄H₅₆N₂ 
• 1301743-12-3 C₇₈H₅₆N₂ 
• 1301743-09-8 C₆₄H₄₄N₂ 
• 1301742-95-9 C₆₂H₃₈N₂ 
• 305350-55-4 1,4-bis(2-(trimethylsilylethynyl)phenylethynyl)benzene 
• 305350-56-5 1,4-bis(2-ethynylphenylethynyl)benzene 

Relevant articles and documents

OFF/ON switching of circularly polarized luminescence by oxophilic interaction of homochiral sulfoxide-containing o-OPEs with metal cations

Here we describe a new class of CPL switches based on oxophilic interactions between chiral sulfoxide-containing ortho-phenylene ethynylene (o-OPE) foldamers and cationic metals. These systems represent a unique case combining high glum values

Chirality Sensing with Stereodynamic Biphenolate Zinc Complexes

Two bidentate ligands consisting of a fluxional polyarylacetylene framework with terminal phenol groups were synthesized. Reaction with diethylzinc gives stereodynamic complexes that undergo distinct asymmetric transformation of the first kind upon binding of chiral amines and amino alcohols. The substrate-to-ligand chirality imprinting at the zinc coordination sphere results in characteristic circular dichroism signals that can be used for direct enantiomeric excess (ee) analysis. This chemosensing approach bears potential for high-throughput ee screening with small sample amounts and reduced solvent waste compared to traditional high-performance liquid chromatography methods. Chirality 27:700-707, 2015.

Enantioselective sensing of chiral amino alcohols with a stereodynamic arylacetylene-based probe

Enantioselective induced circular dichroism analysis of amino alcohols has been accomplished using a conformationally flexible arylacetylene-based probe exhibiting two terminal aldehyde groups. The chirality of the amino alcohol substrates is imprinted on

Chiroptical sensing of citronellal: Systematic development of a stereodynamic probe using the concept of isostericity

A rationally designed stereodynamic ICD probe carrying two terminal amino functions for chemo- and enantioselective sensing of citronellal is introduced. The sensor shows strong Cotton effects upon diimine formation which can be used for accurate ee deter

A Stereodynamic probe providing a chiroptical response to substrate-controlled induction of an axially chiral arylacetylene framework

A stereodynamic probe containing a central 1,4-di(phenylethynyl)benzene rod and two 2-formylphenylethynyl branches has been prepared through a series of Sonogashira cross-coupling reactions with 62% overall yield. This CD silent diarylacetylene-based fram

Enantioselective sensing of amines based on [1 + 1]-, [2 + 2]-, and [1 + 2]-condensation with fluxional arylacetylene-derived dialdehydes

Four induced circular dichroism (ICD) probes exhibiting a stereodynamic arylacetylene framework and terminal aldehyde units have been prepared. The CD silent sensors generate a strong chiroptical response to substrate-controlled induction of axial chirality upon selective [1 + 1]-, [2 + 2]-, and [1 + 2]-condensation. The intense Cotton effects can be exploited for in situ ICD analysis of the absolute configuration and ee of a wide range of amines.

Synthesis of silafluorenes by iridium-catalyzed [2 + 2 + 2] cycloaddition of silicon-bridged diynes with alkynes

(Chemical Equation Presented) Silicon-bridged 1,6-diynes underwent [2 + 2 + 2] cycloaddition with alkynes in the presence of an iridium(I)-phosphine catalyst to afford densely substituted silafluorene derivatives. Extended silafluorene skeletons were cons