5471-84-1

Usage

Uses

1. Used in Chemical Synthesis:
1,4-Bis-(2-broMo-ethoxy)-benzene is used as a key intermediate in the synthesis of various organic compounds, particularly in the preparation of liquid-crystalline pillar[5]and pillar[6]arenes. These pillararenes are important building blocks for the development of advanced materials with unique properties, such as liquid crystals, which have applications in display technologies and sensors.
2. Used in Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, 1,4-Bis-(2-broMo-ethoxy)-benzene could potentially be used in the pharmaceutical industry as a starting material for the synthesis of various drug candidates. Its bromine-ethoxy substituents may allow for further functionalization and modification to create compounds with specific biological activities.
3. Used in Material Science:
In the field of material science, 1,4-Bis-(2-broMo-ethoxy)-benzene could be utilized in the development of novel materials with tailored properties. Its ability to form liquid-crystalline structures may lead to the creation of new materials with enhanced optical, electronic, or mechanical properties, which could be applied in various industries, such as electronics, aerospace, or automotive.
4. Used in Research and Development:
1,4-Bis-(2-broMo-ethoxy)-benzene may also be employed in research and development settings, where it can be used to study the effects of different functional groups on the properties of organic compounds. This knowledge can be applied to design and synthesize new molecules with specific characteristics, potentially leading to breakthroughs in various scientific and technological fields.

InChI:InChI=1/C10H12Br2O2/c11-5-7-13-9-1-2-10(4-3-9)14-8-6-12/h1-4H,5-8H2

Upstream product

• 106-93-4 ethylene dibromide 
• 123-31-9 hydroquinone 
• 104-38-1 1,4-bis(2-hydroxyethoxy)benzene 

Downstream Products

• 106631-39-4 1,4-bis{(N,N-diethyl-amino)-1-oxapropyl}-c-benzene 
• 167647-23-6 1,4,8,11-tetra(2-bromoethoxy)-13b,13c-diphenyl-5,7,12,13b,13c,14-hexahydro-5a,6a,12a,13a-tetraazabenzo[5,6]azuleno[2,1,8-ija]benzo[f]azulene-6,13-dione 
• 1350450-17-7 C₂₀H₂₈Br₂O₂Si₂ 
• 1350450-18-8 C₂₀H₂₈N₆O₂Si₂ 
• 1350450-19-9 C₄₀H₅₀N₈O₂Si₂ 
• 1350450-20-2 C₃₄H₃₄N₈O₂ 
• 1350450-22-4 C₃₆H₄₀N₆O₂Si₂ 
• 1350450-23-5 C₃₀H₂₄N₆O₂ 
• 1166986-84-0 1,4-bis(2-azidoethoxy)benzene 

Relevant academic research and scientific papers

Tetrahedral metal-organic cages with cube-like cavities for selective encapsulation of fullerene guests and their spin-crossover properties

Tetrahedral FeII4L6 coordination cages containing organic linkers with rigid π-electron aromatic rings and flexible alkyl units were constructed. Interestingly, these tetrahedral cages have rare cube-like cavities for selective encapsulation of fullerene guests. In addition, the solid state spin-crossover properties were influenced by guest binding of fullerene C60.

Acid-controlled release complexes of podophyllotoxin and etoposide with acyclic cucurbit[n]urils for low cytotoxicity

The targeted or responsive systems are appealing therapeutic platforms for the development of next-generation precision medications. So, we design and prepare acid-controlled release complexes of podophyllotoxin (POD) and etoposide (VP-16) with pH-labile

Electrochemiluminescent Chiral Discrimination with a Pillar[5]arene Molecular Universal Joint-Coordinated Ruthenium Complex

A bicyclic pillar[5]arene derivative fused with a bipyridine side ring, a so-called molecular universal joint (MUJ), was synthesized, and the pair of enantiomers was resolved by high-performance liquid chromatography enantioresolution. The electrochemilum

Pillar[5]arene-mediated synthesis of gold nanoparticles: Size control and sensing capabilities

We present a simple procedure for the synthesis of quasi-spherical Au nanoparticles in a wide size range mediated by macrocyclic host molecules, ammonium pillar[5]arene (AP[5]A). The strategy is based on a seeded growth process in which the water-soluble

Synthesis and applications of copillar[5]arene dithiols

A novel copillar[4+1]arene incorporating alkylthiol substituents was synthesised in three steps and structurally characterised as the first example of a pillar[n]arene to incorporate two terminal thiols on the same aromatic ring. The macrocycle was attach

A co-pillar[5]arene sensor for linear biogenic amines

A thiolated co-pillar[5]arene was attached to the surface of a gold electrode and shown to give an analyte-selective voltammetric response to linear biogenic amines.

Facile surface functionalization of upconversion nanoparticles with phosphoryl pillar[5]arenes for controlled cargo release and cell imaging

Upon surface functionalization and stabilization of β-NaYF4:Yb/Er upconversion nanoparticles (UCNPs) with phosphoryl pillar[5]arenes (PP5) via a facile ligand exchange method, we constructed a new hybrid material (PP5-UCNPs) with good water dis

The chiral interfaces fabricated by d/l-alanine-pillar[5]arenes for selectively adsorbing ctDNA

In this paper, the d/l-AP5-interfaces are firstly fabricated by attaching d-alanine-pillar[5]arene and l-alanine-pillar[5]arene (d/l-AP5) onto the gold surface, and they exhibit a significantly different chiral influence on the morphology and the adsorpti

Two N-heterocyclic carbene silver(I) cyclophanes: Synthesis, structural studies, and recognition for p -phenylenediamine

The diimidazolium salt 1,5-bis[1-ethylimidazoliumylethoxy]naphthalene hexafluorophosphate (2) and the dibenzimidazolium salt 1,4-bis[1-(n-butyl) benzimidazoliumylethoxy]benzene hexafluorophosphate (4), as well as their N-heterocyclic carbene silver(I) cyc

Metallosupramolecules of pillar[5]-bis-trithiacrown including a mercury(ii) iodide ion-triplet complex

A combination of pillar[5]-bis-trithiacrown (L) and mercury(ii) halides afforded a monomer complex (Cl-form), a 1-D coordination polymer (Br-form) and a supramolecular ion-triplet complex [(I·Hg·I)@L] (I-form). In the ion-triplet complex, the host encapsu