14691-89-5

  • Product Name:4-ACETAMIDO-TEMPO
  • Molecular Formula:C11H21N2O2
  • Purity:99%
  • Molecular Weight:215.316
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Product Details

Buy Good Quality 4-ACETAMIDO-TEMPO 14691-89-5 with a minimum purity of 99%

  • Molecular Formula:C11H21N2O2
  • Molecular Weight:215.316
  • Appearance/Colour:Orange-red crystalline powder 
  • Vapor Pressure:1.9E-06mmHg at 25°C 
  • Melting Point:143-145 °C(lit.) 
  • Refractive Index:1.506 
  • Boiling Point:368.8 °C at 760 mmHg 
  • Flash Point:176.8 °C 
  • PSA:32.34000 
  • Density:1.06g/cm3 
  • LogP:1.81840 

4-ACETAMIDO-TEMPO(Cas 14691-89-5) Usage

Purification Methods

Dissolve the 1-oxyl in CH2Cl2, wash it with saturated K2CO3, then saturated aqueous NaCl, dry (Na2SO4), filter and evaporate. The red solid is recrystallised from aqueous MeOH, m 147.5o. [Ma & Bobbitt J Org Chem 56 6110 1991, Rozantsev & Kokhanov Bull Acad Sci USSR, Div Chem Sci 15 1422 1966, Beilstein 22/8 V 174.]

General Description

4-Acetamido-2,2,6,6-tetramethylpiperidine 1-oxyl undergoes one-electron oxidation and reduction reactions. Reaction products were analyzed by 1H, 13C and 15N NMR spectral data.

InChI:InChI=1/C11H22N2O2/c1-8(14)12-9-6-10(2,3)13(15)11(4,5)7-9/h9,15H,6-7H2,1-5H3,(H,12,14)

14691-89-5 Relevant articles

Preparation of Some Homologous TEMPO Nitroxides and Oxoammonium Salts; Notes on the NMR Spectroscopy of Nitroxide Free Radicals; Observed Radical Nature of Oxoammonium Salt Solutions Containing Trace Amounts of Corresponding Nitroxides in an Equilibrium Relationship

Bobbitt, James M.,Eddy, Nicholas A.,Cady, Clyde X.,Jin, Jing,Gascon, Jose A.,Gelpí-Dominguez, Svetlana,Zakrzewski, Jerzy,Morton, Martha D.

, p. 9279 - 9290 (2017/09/22)

Three new homologous TEMPO oxoammonium s...

Synthesis and fluorescence properties of six fluorescein-nitroxide radical hybrid-compounds

Sato, Shingo,Endo, Susumu,Kurokawa, Yusuke,Yamaguchi, Masaki,Nagai, Akio,Ito, Tomohiro,Ogata, Tateaki

supporting information, p. 66 - 71 (2016/07/06)

Six fluorescein-nitroxide radical hybrid...

Kinetics and thermodynamics of reversible disproportionation-comproportionation in redox triad oxoammonium cations - Nitroxyl radicals - Hydroxylamines

Sen, Vasily D.,Tikhonov, Ivan V.,Borodin, Leonid I.,Pliss, Evgeny M.,Golubev, Valery A.,Syroeshkin, Mikhail A.,Rusakov, Alexander I.

, p. 17 - 24 (2015/03/03)

Kinetics and equilibrium of the acid-cat...

Selective Aromatic C-H Hydroxylation Enabled by η6-Coordination to Iridium(III)

D'Amato, Erica M.,Neumann, Constanze N.,Ritter, Tobias

, p. 4626 - 4631 (2015/10/06)

We report an aromatic C-H hydroxylation ...

14691-89-5 Process route

piperidine
110-89-4

piperidine

5-phenylbenzoxazole
201415-38-5

5-phenylbenzoxazole

4-acetylamino-2,2,6,6-tetramethylpiperidine-1-oxoammonium tetrafluoroborate

4-acetylamino-2,2,6,6-tetramethylpiperidine-1-oxoammonium tetrafluoroborate

5-phenyl-2-(piperidin-1-yl)benzoxazole
1204006-30-3

5-phenyl-2-(piperidin-1-yl)benzoxazole

4-acetylamino-2,2,6,6-tetramethyl-1-piperidinoxy
14691-89-5,136708-39-9

4-acetylamino-2,2,6,6-tetramethyl-1-piperidinoxy

Conditions
Conditions Yield
piperidine; 5-phenylbenzoxazole; With scandium tris(trifluoromethanesulfonate); In acetonitrile; at 60 ℃; for 6h;
4-acetylamino-2,2,6,6-tetramethylpiperidine-1-oxoammonium tetrafluoroborate; With 2,2,6,6-tetramethyl-piperidine; In acetonitrile; at 60 ℃; for 0.166667h;
138 mg
105 mg
ethylenediaminetetraacetic acid disodium salt dihydrate

ethylenediaminetetraacetic acid disodium salt dihydrate

N-(2,2,6,6-tetramethylpiperidin-4-yl)acetamide
40908-37-0

N-(2,2,6,6-tetramethylpiperidin-4-yl)acetamide

4-acetylamino-2,2,6,6-tetramethylpiperidine-N-oxyl
14691-89-5

4-acetylamino-2,2,6,6-tetramethylpiperidine-N-oxyl

Conditions
Conditions Yield
With ammonium carbonate; dihydrogen peroxide; In water;
97.5%
With dihydrogen peroxide; sodium hydrogencarbonate; In water;
With dihydrogen peroxide; sodium carbonate; In water;

14691-89-5 Upstream products

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    40908-37-0

    N-(2,2,6,6-tetramethylpiperidin-4-yl)acetamide

  • 136708-42-4
    136708-42-4

    4-(acetylamino)-2,2,6,6-tetramethyl-1-hydroxy-piperidinium p-toluenesulfonate

  • 136708-43-5
    136708-43-5

    4-acetylamino-2,2,6,6-tetramethyl-1-piperidinium acetate

  • 14691-88-4
    14691-88-4

    4-amino-2,2,6,6-tetramethyl-1-piperidine-1-oxyl

14691-89-5 Downstream products

  • 14691-88-4
    14691-88-4

    4-amino-2,2,6,6-tetramethyl-1-piperidine-1-oxyl

  • 122586-91-8
    122586-91-8

    N-(1-Cyclohexyloxy-2,2,6,6-tetramethylpiperidin-4-yl)acetamide

  • 14691-88-4
    14691-88-4

    4-amino-2,2,6,6-tetramethylpiperidinyloxy

  • 1350920-13-6
    1350920-13-6

    4-acetamido-2,2,6,6-tetramethylpiperidine-N-hydroxyammonium tetrafluoroborate

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