CAS 14691-89-5
:4-Acetamido-TEMPO
- 1-Oxyl-2,2,6,6-tetramethyl-4-acetamidopiperidine
- 1-Piperidinyloxy radical,4-(acetylamino)-2,2,6,6-tetramethyl-
- 1-Piperidinyloxy, 4-(acetylamino)-2,2,6,6-tetramethyl-
- 2,2,6,6-Tetramethyl-4-acetamidopiperidin-1-oxyl
- 2,2,6,6-Tetramethyl-4-acetamidopiperidine-1-oxyl
- 2,2,6,6-Tetramethyl-4-acethylamino-piperidin-1-oxyl
- 2,2,6,6-Tetramethyl-4-acetylaminopiperidin-1-oxyl
- 4-(Acetylamino)-2,2,6,6-Tetramethyl-1-Piperidinylox
- 4-(Acetylamino)-2,2,6,6-tetramethylpiperidin-1-oxyl
- 4-(Acetylamino)-2,2,6,6-tetramethylpiperidin-1-yloxyl
- 4-(acetylamino)-2,2,6,6-tetramethyl-1-Piperidinyloxy
- 4-Acetamide-2,2,6,6-tetramethyl-1-piperidin-yloxy
- 4-Acetamido-1-oxyl-2,2,6,6-tetramethylpiperidine
- 4-Acetamido-2,2,6,6-tetramethyl-1-piperidinyloxy
- 4-Acetamido-2,2,6,6-tetramethyl-1-piperidinyloxyl
- 4-Acetamido-2,2,6,6-tetramethylpiperidin-1-oxy
- 4-Acetamido-2,2,6,6-tetramethylpiperidin-1-oxyl
- 4-Acetamido-2,2,6,6-tetramethylpiperidine-1-oxyl
- 4-Acetamido-2,2,6,6-tetramethylpiperidinooxy
- 4-Acetamido-2,2,6,6-tetramethylpiperidinyloxy
- 4-Acetamido-4,4,5,5-tetramethylpiperidin-1-oxyl
- 4-Acetamino-2,2,6,6-tetramethylpiperidine-1-oxyl
- 4-Acetamino-2,2,6,6-tetramethylpiperidine-N-oxyl
- 4-Acetamino-2,2,6,6-tetramethylpiperidinyloxy
- 4-Acetoamido-2,2,6,6,-tetramethylpiperidine 1-oxyl
- 4-Acetoamino(2,2,6,6-tetramethylpiperidin-1-yl)oxyl
- 4-Acetylamino-2,2,6,6-tetramethylpiperidine N-oxyl
- 4-Acetylamino-TEMPO
- 4-N-Acetylamino-TEMPO
- Acetamide-TEMPO
- Acetamido-TEMPO
- N-(1-Hydroxy-2,2,6,6-tetramethyl-4-piperidinyl)acetamide
- N-(1-Oxyl-2,2,6,6-tetramethylpiperidin-4-yl)acetamide
- N-(1-hydroxy-2,2,6,6-tetramethylpiperidin-4-yl)acetamide
- Piperidinooxy, 4-acetamido-2,2,6,6-tetramethyl-
- Tempace
- Vedi altri sinonimi
4-Acetamido-TEMPO, free radical, 98+%
CAS:4-Acetamido-TEMPO, free radical oxidizes alcohols to carbonyl compounds in the presence of TsOH. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar pro
Formula:C11H21N2O2Purezza:98+%Colore e forma:Orange to red, Crystals or powder or crystalline powderPeso molecolare:213.304-(Acetylamino)-2,2,6,6-tetramethyl-1-piperidinyloxy
CAS:Formula:C11H21N2O2Purezza:98%Colore e forma:SolidPeso molecolare:213.29664-Acetamido-2,2,6,6-tetramethylpiperidine 1-oxyl
CAS:4-Acetamido-2,2,6,6-tetramethylpiperidine 1-oxylFormula:C11H21N2O2Purezza:98%Colore e forma: light yellow to orange solidPeso molecolare:213.30g/mol4-Acetamido-2,2,6,6-tetramethylpiperidine 1-Oxyl Free Radical [Catalyst for Oxidation]
CAS:Formula:C11H21N2O2Purezza:>98.0%(GC)Colore e forma:Light yellow to Brown powder to crystalinePeso molecolare:213.304-Acetamido-2,2,6,6-tetramethylpiperidine 1-oxyl
CAS:Formula:C11H21N2O2Purezza:95.0%Colore e forma:SolidPeso molecolare:213.164-Acetamido-2,2,6,6-Tetramethylpiperidine-1-Oxyl (Acetamido TEMPO) pure, 97%
CAS:Formula:C11H21N2O2Purezza:min. 97%Colore e forma:Orange to red to brown to orange- red, Powder, ClearPeso molecolare:213.304-Acetamido-2,2,6,6-tetramethylpiperidine-1-oxyl
CAS:4-Acetamido-2,2,6,6-tetramethylpiperidine-1-oxyl (ATMP) is a synthetic compound that has been used for the preparation of biomolecules. ATMP is prepared in two steps from hexane and acetonitrile. The first step involves protonation of the nitrile group to form an acetamido group followed by condensation with a piperidone ring. The second step involves addition of a chloride ion to form an ester. ATMP can be used as a solvent in preparative methods because it is insoluble in water and has low energy interactions. In addition, this molecule's hydrophobic character allows it to interact with hydrodynamic interactions.
Formula:C11H21N2O2Purezza:Min. 98 Area-%Peso molecolare:213.3 g/mol






