2-Phenoxyaniline

CAS No.: 2688-84-8

product details:

Purity: 99%

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Factory Sells Best Quality 2-Phenoxyaniline 2688-84-8 with USP

  • Molecular Formula: C12H11NO
  • Molecular Weight: 185.225
  • Appearance/Colour: White to light yellow crystal powder 
  • Melting Point: 47-49 °C(lit.) 
  • Refractive Index: 1.5300 (estimate) 
  • Boiling Point: 296.4 °C at 760 mmHg 
  • PKA: 3.78±0.10(Predicted) 
  • Flash Point: 131.8 °C 
  • PSA: 35.25000 
  • Density: 1.141 g/cm3 
  • LogP: 3.64230 

2-Phenoxyaniline(Cas 2688-84-8) Usage

General Description

2-Phenoxyaniline forms crystalline 2:1 (host-to-guest) inclusion complexes with β-cyclodextrin.

InChI:InChI=1/C12H11NO/c13-11-8-4-5-9-12(11)14-10-6-2-1-3-7-10/h1-9H,13H2

2688-84-8 Relevant articles

Highly robust magnetically recoverable Ag/Fe2O3 nanocatalyst for chemoselective hydrogenation of nitroarenes in water

Patra, Astam K.,Vo, Nhat Tri,Kim, Dukjoon

, p. 148 - 156 (2017)

This work reports on additive-free Ag na...

Exploration of Fragment Binding Poses Leading to Efficient Discovery of Highly Potent and Orally Effective Inhibitors of FABP4 for Anti-inflammation

Su, Haixia,Zou, Yi,Chen, Guofeng,Dou, Huixia,Xie, Hang,Yuan, Xiaojing,Zhang, Xianglei,Zhang, Naixia,Li, Minjun,Xu, Yechun

, p. 4090 - 4106 (2020/05/20)

Fatty-acid binding protein 4 (FABP4) is ...

Copper complexes of 1,4-diazabutadiene ligands: Tuning of metal oxidation state and, application in catalytic C-C and C-N bond formation

Mukherjee, Aparajita,Basu, Semanti,Bhattacharya, Samaresh

, (2019/11/11)

Reaction of 1,4-diazabutadiene (p-RC6H4N...

A 3 - benzofuran bromine two synthetic method (by machine translation)

-

Paragraph 0049; 0052; 0053, (2019/07/10)

The invention relates to a 3 - benzofura...

COMPOUND AND ORGANIC ELECTRONIC DEVICE USING THE SAME

-

Paragraph 0078; 0079; 0082, (2019/04/14)

Provided are a novel compound and an org...

2688-84-8 Process route

diphenylether
101-84-8

diphenylether

4,4'-oxydiphenylene diamine
101-80-4,121509-79-3

4,4'-oxydiphenylene diamine

4-phenoxyanilin
139-59-3

4-phenoxyanilin

2-phenoxyaniline
2688-84-8

2-phenoxyaniline

Conditions
Conditions Yield
With O-(4-nitrobenzoyl)hydroxylammonium trifluoromethanesulfonate; iron(II) bromide; silver(I) triflimide; In 2,2,2-trifluoroethanol; water; at 30 ℃; for 2h;
39.5%
19.8%
19.8%
diphenylether
101-84-8

diphenylether

4-phenoxyanilin
139-59-3

4-phenoxyanilin

2-phenoxyaniline
2688-84-8

2-phenoxyaniline

Conditions
Conditions Yield
diphenylether; With pyridine; trifluorormethanesulfonic acid; tetrabutylammonium tetrafluoroborate; In acetonitrile; at 25 ℃; Electrochemical reaction;
With piperidine; In acetonitrile; at 80 ℃; for 12h; Overall yield = 92 %; Electrochemical reaction;
53%
40%
With 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; 3,6‐di‐tert‐butyl‐9‐mesityl‐10‐phenylacridin‐10‐ium tetrafluoroborate; oxygen; ammonium carbamate; In water; 1,2-dichloro-ethane; at 23 ℃; for 24h; Overall yield = 62 %; regioselective reaction; Irradiation;

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