2496-26-6

Basic information

• Product Name: 4'-Ethoxyazobenzene-4-ol
• Synonyms: 4-(4-Ethoxyphenylazo)phenol;4-[(4-Ethoxyphenyl)azo]phenol;4'-Ethoxyazobenzene-4-ol;4-Hydroxy-4'-ethoxyazobenzene
• CAS NO: 2496-26-6
• Molecular Formula: C₁₄H₁₄N₂O₂
• Molecular Weight: 242.2732
• Mol File: 2496-26-6.mol
• Article Data: 15

Chemical Properties

• Melting Point: 127 °C(Solv: methanol (67-56-1); water (7732-18-5))
• Boiling Point: 380.6°Cat760mmHg
• Flash Point: 184°C
• Appearance: /
• Density: 1.13g/cm³
• Vapor Pressure: 5.38E-06mmHg at 25°C
• Refractive Index: 1.571
• PKA: 8.81±0.15(Predicted)
• CAS DataBase Reference: 4'-Ethoxyazobenzene-4-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 4'-Ethoxyazobenzene-4-ol(2496-26-6)
• EPA Substance Registry System: 4'-Ethoxyazobenzene-4-ol(2496-26-6)

Safety Data

• Hazardous Substances Data: 2496-26-6(Hazardous Substances Data)

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

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

Downstream Products

• 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 
• 244073-03-8 (E)-4-hexyloxy-4'-ethoxyazobenzene 
• 101902-36-7 4-[6-(methacryloyloxy)hexyloxy]-4'-ethoxyazobenzene 
• 156-43-4 4-Ethoxyaniline 
• 912646-02-7 3,5-bis{6-[4-(4'-ethoxyphenylazo)phenoxy]hexyloxy}benzyl alcohol 
• 912646-01-6 [4-(6-bromo-hexyloxy)-phenyl]-(4-ethoxy-phenyl)-diazene 

Relevant articles and documents

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

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

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