2496-26-6

Usage

InChI:InChI=1/C14H14N2O2/c1-2-18-14-9-5-12(6-10-14)16-15-11-3-7-13(17)8-4-11/h3-10,16H,2H2,1H3

Upstream product

• 156-43-4 4-Ethoxyaniline 
• 108-95-2 phenol 
• 38793-99-6 4-ethoxy-benzenediazonium; chloride 
• 19262-82-9 4-ethoxybenzenediazonium 
• 100-29-8 1-ethoxy-4-nitrobenzene 
• 637-56-9 4-ethoxyaniline hydrochloride 
• 100-02-7 4-nitro-phenol 

Downstream Products

• 20730-67-0 p-(ethoxyphenyl azophenyl) valerate 
• 38974-22-0 p-(ethoxyphenyl azophenyl) acetate 
• 62640-51-1 4-(4-Ethoxy-phenyl-ONN-azoxy)-phenol 
• 912646-01-6 [4-(6-bromo-hexyloxy)-phenyl]-(4-ethoxy-phenyl)-diazene 
• 156-43-4 4-Ethoxyaniline 
• 850706-08-0 4-ethoxy-4'-(6-hydroxyhex-1-yloxy)azobenzene 
• 1234555-20-4 4-ethoxy-4'-(2-(2-bromoisobutyryloxy)ethoxy)azobenzene 
• 301299-32-1 4-hydroxyethoxy-4'-ethoxyazobenzene 
• 588-52-3 4,4'-diethoxyazoxybenzene 

Relevant academic research and scientific papers

Pathway-Dependent Phase Transitions of Supramolecular Self-assemblies Containing Cationic Amphiphiles with Azobenzene and Disulfide Groups

There have been several attempts to construct supramolecular chemical systems that mimic the phase transitions in living systems. However, most of these phase transitions are one-to-one and induced by one stimulus or chemical; there have been few reports

Reversible photocontrol of DNA coacervation

Coacervate micro-droplets produced by liquid-liquid phase separation are increasingly used to emulate the dynamical organization of membraneless organelles found in living cells. Designing synthetic coacervates able to be formed and disassembled with impr

Covalent Adaptable Liquid Crystal Networks Enabled by Reversible Ring-Opening Cascades of Cyclic Disulfides

The development of covalent adaptable liquid crystal networks (LCNs) enabled by introducing dynamic covalent bonds has endowed liquid crystal actuators with self-healing properties and reversible shape programmability, broadening their applications in div

Synthesis, mesomorphic and dielectric properties of 4-(cyanomethoxy)phenyl 4-alkoxybenzoates, 4-(cyanomethoxy)-4′-alkoxyazo- and -azoxybenzenes

Preparation methods were developed for homologs of 4-(cyanomethoxy)phenyl 4-alkoxybenzoates (C7, C8, C9), 4-(cyanomethoxy)-4′-alkoxyazo (C2, C3, C 6), -azoxybenzenes (C3, C6) whose composition and structure were proved by elemental analysis and 1H NMR spectra. 4-(Cyanomethoxy) group destabilizes the mesophase, consequently, only four among the compounds obtained exhibit the thermotropic nematic mesomorphism.

Double "plug and play" templates technology for photo controllable drug release polyelectrolyte multilayers

An approach for the generation of photo controllable drug release polyelectrolyte multilayers is developed by combining double "plug and play" (PnP) templates technology and host-guest chemistry. These multilayers exhibited a reversible drug loading and r

Photocontrolled microphase separation in a nematic liquid-crystalline diblock copolymer

Using a bromo-terminated poly(ethylene oxide) as a macroinitiator, an amphiphilic liquid-crystalline (LC) diblock copolymer with an azobenzene moiety as a nematic mesogen was prepared by an atom transfer radical polymerization process. In thin films of th

Water-soluble triply-responsive homopolymers of N,N-Dimethylaminoethyl methacrylate with a terminal azobenzene moiety

Novel water-soluble triply-responsive homopolymers of N,N- dimethylaminoethyl methacrylate (DMAEMA) containing an azobenzene moiety as the terminal group were synthesized by atom transfer radical polymerization (ATRP) technique. The ATRP process of DMAEMA

Photoalignment and holographic properties of azobenzene-containing block copolymers with oxyethylene and alkyl spacers

Two azobenzene-containing block copolymers with an oxyethylene (P1) or an alkyl (P2) spacer in the side chain were prepared by atom transfer radical polymerization (ATRP). Neither of the block copolymers with a low azobenzene content showed a liquid-cryst

Colloidal sphere formation, H-aggregation, and photoresponsive properties of an amphiphilic random copolymer bearing branched Azo side chains

This work studied the colloidal sphere formation, H-aggregation, and photoresponsive properties of an amphiphilic random copolymer functionalized with branched azo side chains (POAPB6P-AC). The colloidal spheres were prepared through gradual hy

Mesogenic biphenyl derivatives with azo and ester central linkage

Biphenyl nucleus comprises one of the most interesting research areas in the study of relations between chemical constitution and mesomorphic properties. Few biphenyl derivatives with azo and ester central linkage having following general formula have been synthesized and their mesomorphic properties were evaluated. Where R=-H, -OCH3, R'=-CH3, -OCH3, -OC2H5, -OC4H9; X=-H, -Br. All the synthesized compounds were characterized by elemental analysis and spectroscopic methods.