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4'-Ethoxyazobenzene-4-ol, also known as 4-(4-ethoxyphenylazo)phenol, is an organic compound with the chemical formula C14H14N2O2. It is a yellow crystalline solid that is soluble in organic solvents such as ethanol and ether. 4'-Ethoxyazobenzene-4-ol is primarily used as a chemical intermediate in the synthesis of various dyes and pigments, particularly those with azo structures. It is also employed in the production of certain pharmaceuticals and as a reagent in analytical chemistry. Due to its potential applications and reactivity, 4'-Ethoxyazobenzene-4-ol is a significant compound in the field of organic chemistry.

2496-26-6

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2496-26-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2496-26-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,9 and 6 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2496-26:
(6*2)+(5*4)+(4*9)+(3*6)+(2*2)+(1*6)=96
96 % 10 = 6
So 2496-26-6 is a valid CAS Registry Number.
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

2496-26-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[(4-ethoxyphenyl)hydrazinylidene]cyclohexa-2,5-dien-1-one

1.2 Other means of identification

Product number -
Other names Phenol,4-((4-ethoxyphenyl)azo)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2496-26-6 SDS

2496-26-6Relevant academic research and scientific papers

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

Sawada, Daichi,Asakura, Kouichi,Banno, Taisuke

, p. 13840 - 13845 (2021)

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

Lafon, Suzanne,Martin, Nicolas

, p. 329 - 351 (2020/07/15)

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

Bisoyi, Hari K.,Huang, Shuai,Li, Quan,Liu, Zhongcheng,Shen, Yikang,Tao, Yu,Wang, Meng,Yang, Hong

supporting information, p. 12543 - 12551 (2021/08/03)

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

Kuvshinova,Burmistrov,Novikov,Litov,Aleksandriiskii,Koifman

, p. 615 - 620 (2014/07/08)

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

Wu, Ming,Cao, Yiping,Zhang, Xianzheng,Zhang, Yuanfang,Chen, Yong,He, Liu,Qian, Zhiyong

supporting information, p. 9846 - 9848 (2012/11/13)

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

Yu, Haifeng,Kobayashi, Takaomi,Hu, Guo-Hua

experimental part, p. 1554 - 1561 (2012/02/13)

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

Tang, Xinde,Liang, Xiaochao,Gao, Longcheng,Fan, Xinghe,Zhou, Qifeng

experimental part, p. 2564 - 2570 (2011/04/16)

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

Naka, Yumiko,Yu, Haifeng,Shishido, Atsushi,Ikeda, Tomiki

scheme or table, p. 131 - 141 (2010/08/06)

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

Deng, Yonghong,Li, Yaobang,Wang, Xiaogong

, p. 6590 - 6598 (2007/10/03)

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

Prajapati

, p. 769 - 777 (2007/10/03)

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.

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