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2216-12-8

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2216-12-8 Usage

Chemical Properties

CLEAR YELLOW TO BROWN LIQUID

Safety Profile

Moderately toxic by intravenousroute. When heated to decomposition it emits toxic fumesof NOx.

Purification Methods

Purify the ether by fractional disillation. UV (EtOH): 255, 315mm ( 6200 and 2800), IR (CS2): 1350 (NO2) and 1245, 1265 (COC) cm-1 [UV, IR: Dahlgard & Brewster J Am Chem Soc 80 5861 1958, Tomita & Takase Yakugaku Zasshi (J Pharm Soc Japan) 75 1077 1955, Fox & Turner J Chem Soc 1115 1930, Henley J Chem Soc 1222 1930]. [Beilstein 6 H 218, 6 II 210, 6 III 801.]

Check Digit Verification of cas no

The CAS Registry Mumber 2216-12-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,1 and 6 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2216-12:
(6*2)+(5*2)+(4*1)+(3*6)+(2*1)+(1*2)=48
48 % 10 = 8
So 2216-12-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H9NO3/c14-13(15)11-8-4-5-9-12(11)16-10-6-2-1-3-7-10/h1-9H

2216-12-8 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (A18088)  2-Nitrophenyl phenyl ether, 99%   

  • 2216-12-8

  • 10g

  • 418.0CNY

  • Detail
  • Alfa Aesar

  • (A18088)  2-Nitrophenyl phenyl ether, 99%   

  • 2216-12-8

  • 50g

  • 1744.0CNY

  • Detail
  • Alfa Aesar

  • (A18088)  2-Nitrophenyl phenyl ether, 99%   

  • 2216-12-8

  • 250g

  • 7439.0CNY

  • Detail
  • Sigma-Aldrich

  • (73307)  2-Nitrophenylphenylether  Selectophore, ≥99.0%

  • 2216-12-8

  • 73307-5ML

  • 1,378.26CNY

  • Detail

2216-12-8Relevant articles and documents

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Henley

, p. 1222 (1930)

-

Heterogeneous O -arylation of nitroarenes with substituted phenols over a copper immobilized mesoporous silica catalyst

Maity, Tanmoy,Bhunia, Susmita,Das, Soma,Koner, Subratanath

, p. 33380 - 33386 (2016)

Highly porous and robust mesoporous silica, SBA-15 has been subjected to post-synthesis modification for the anchoring of copper through Schiff base moiety formation using the silicon alkoxide route. The hybrid porous material has been fully characterized by powder-XRD, electronic spectra, EPR, thermogravimetric analysis, N2 sorption measurements, and TEM and SEM/EDS studies. The efficiency of the catalyst has been assessed in the O-arylation reaction using various substituted phenols and nitroarenes in heterogeneous conditions. The catalytic coupling reaction efficiently produces unsymmetrical diaryl ethers. The impressive capability to activate substrates having electron-donating or electron-withdrawing substituents and to have a high turnover frequency in the catalytic reactions made the catalyst highly desirable.

Preparation method of secondary aromatic amine

-

Paragraph 0014, (2021/03/31)

The invention provides a method for preparing secondary aromatic amine by performing a palladium-catalyzed C-N coupling reaction on (pseudo)aryl halide and (pseudo)heterocyclic aryl halide and primary(heterocyclic)aromatic amine. The method is characterized in that an alkali for promoting the reaction is an alkali metal carboxylate or an alkali metal bicarbonate.

Thermally stable and robust gadolinium-based metal-organic framework: Synthesis, structure and heterogeneous catalytic O-arylation reaction

Ghosh, Pameli,Maity, Tanmoy,Biswas, Saptarshi,Debnath, Rakesh,Koner, Subratanath

, (2020/12/21)

Hydrothermal treatment of gadolinium nitrate and 2,6-naphthalenedicarboxylic acid (H2NDC) afforded a new metal-organic framework compound, {[Gd4(NDC)6(H2O)6]·2H2O}n(1). Compound 1 has been characterized by single-crystal X-ray crystallography, elemental analysis, FT-IR spectroscopy, therrmogravimetric analysis (TGA) and powder X-ray diffraction analysis. It is crystallized in the monoclinic system with the P21/n space group. Four crystallographically distinct Gd (III) centres are interconnected with each other through bridged carboxylato oxygen atoms and water molecules to form tetranuclear secondary building units, which are further connected through the carboxylato ligand and the network propagates along the crystallographic ac plane to form a 2D structure. Subsequent reinforcement from the remaining carboxylato oxygen atoms gives rise to a robust 3D framework structure. Thermogravimetric analysis demonstrates that compound 1 is fairly stable after dehydration under a nitrogen atmosphere. Notably, compound 1 is capable of catalyzing the O-arylation reaction efficiently between substituted phenols and bromoarene under heterogeneous conditions at 80 °C to afford unsymmetrical diarylethers.

A novel magnetic polyacrylonotrile-based palladium Core?Shell complex: A highly efficientcatalyst for Synthesis of Diaryl ethers

Eslami, Mohammad,Jarahiyan, Atefeh,Moghaddam, Firouz Matloubi,Pourjavadi, Ali

, (2020/04/15)

The present article describes the synthesis of a new magnetic polyacrylonitrile-based Pd catalyst involving polyacrylonitrile modified via 2-aminopyridine as an efficient support to immobilize Pd nanoparticles. The simple reusability, easy separation and high stability of this Pd complex make it an excellent candidate to generate a C–O bond via Ph-X activation which is a really important subject in achieving biologically active compounds. It is worth to note access to good and high yields as well as broad substrate scope have resulted from superior reactivity of this catalyst complex. Furthermore, the structure of the magnetic polyacrylonitrile-based heterogeneous catalyst was characterized by fourier transmission infrared (FT-IR) spectroscopy, field emission scanning electron microscopy (FE-SEM) and transmission electron microscopy (TEM), X-ray diffraction (XRD). Also, its thermal properties were studied by thermogravimetric analysis (TGA).

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