4-NITROPHENYL PHENYL ETHER

  • Name: 4-NITROPHENYL PHENYL ETHER
  • CAS: 620-88-2
  • Purity: 99%
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Details

Buy Good Quality 4-NITROPHENYL PHENYL ETHER 620-88-2 with a minimum purity of 99%

  • Molecular Formula: C12H9 N O3
  • Molecular Weight: 215.208
  • Appearance/Colour: yellow flakes 
  • Vapor Pressure: 1.36E-06mmHg at 25°C 
  • Melting Point: 53-56 °C(lit.)
     
  • Refractive Index: 1.5750 (estimate) 
  • Boiling Point: 320 °C(lit.)
     
  • Flash Point: >230 °F  
  • PSA： 55.05000 
  • Density: 1.12g/cm3 
  • LogP: 3.91030 

4-NITROPHENYL PHENYL ETHER(Cas 620-88-2) Usage

Synthesis Reference(s)

Tetrahedron Letters, 25, p. 3383, 1984 DOI: 10.1016/S0040-4039(01)91026-3Synthetic Communications, 20, p. 2855, 1990 DOI: 10.1080/00397919008051499

Safety Profile

Mutation data reported. An eyeirritant. When heated to decomposition it emits toxicfumes of NOx.

InChI:InChI=1/C15H16ClNO/c1-10-4-6-13(7-5-10)17-11(2)8-14(12(17)3)15(18)9-16/h4-8H,9H2,1-3H3

620-88-2 Relevant articles

Synthesis and characterization of nano-cellulose immobilized phenanthroline-copper (I) complex as a recyclable and efficient catalyst for preparation of diaryl ethers, N-aryl amides and N-aryl heterocycles

Aghili, Nora,Hosseinzadeh, Rahman,Mavvaji, Mohammad

, (2022/01/03)

Functionalized nanocellulose was prepare...

Suzuki?Miyaura coupling and O?arylation reactions catalysed by palladium(II) complexes of bulky ligands bearing naphthalene core, Schiff base functionality and biarylphosphine moiety

Arora, Aayushi,Kaushal, Jolly,Kumar, Arun,Nautiyal, Divyanshu,Oswal, Preeti,Singh, Siddhant

, (2022/01/19)

Schiff bases L1 [i.e., 2-(diphenylphosph...

Diarylation of N- and O-nucleophiles through a metal-free cascade reaction

Bulfield, David,Kervefors, Gabriella,Linde, Erika,Olofsson, Berit,Purkait, Nibadita

, p. 850 - 865 (2022/03/14)

The arylation of heteroatom nucleophiles...

Ligand- and Counterion-Assisted Phenol O-Arylation with TMP-Iodonium(III) Acetates

Kikushima, Kotaro,Miyamoto, Naoki,Watanabe, Kazuma,Koseki, Daichi,Kita, Yasuyuki,Dohi, Toshifumi

supporting information, p. 1924 - 1928 (2022/03/27)

High reactivity of trimethoxyphenyl (TMP...

620-88-2 Process route

4-nitrophenoxytriphenylbismuth chloride
105071-84-9

4-nitrophenoxytriphenylbismuth chloride

4-nitro-phenol
100-02-7,78813-13-5,89830-32-0

4-nitro-phenol

biphenyl
92-52-4,1594-86-1

biphenyl

4-nitrophenyl phenyl ether
620-88-2

4-nitrophenyl phenyl ether

Conditions
Conditions Yield
In benzene; for 43h; Heating;
27%
19%
2%
sodium phenoxide
139-02-6

sodium phenoxide

4-Nitro-diphenyliodoniumhydroxid
46734-23-0

4-Nitro-diphenyliodoniumhydroxid

p-nitrobenzene iodide
636-98-6

p-nitrobenzene iodide

diphenylether
101-84-8

diphenylether

iodobenzene
591-50-4

iodobenzene

4-nitrophenyl phenyl ether
620-88-2

4-nitrophenyl phenyl ether

Conditions
Conditions Yield
In water; at 60 ℃; Product distribution; Mechanism; relative rates of decomposition of the 9-I-2 intermediate;

620-88-2 Upstream products

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    para-dinitrobenzene

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    100-67-4

    potassium phenolate

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    101-84-8

    diphenylether

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    100-00-5

    4-chlorobenzonitrile

620-88-2 Downstream products

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    15018-23-2

    1,2-bis(4-phenoxyphenyl)diazene oxide

  • 21969-04-0
    21969-04-0

    1-(4-nitrophenoxy)-4-bromobenzene

  • 1836-74-4
    1836-74-4

    4-(4-chlorophenoxy)nitrobenzene

  • 101-63-3
    101-63-3

    bis(4-nitrophenyl)ether

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