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-
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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
Fórmula:C11H21N2O2Pureza:98+%Forma y color:Orange to red, Crystals or powder or crystalline powderPeso molecular:213.304-(Acetylamino)-2,2,6,6-tetramethyl-1-piperidinyloxy
CAS:Fórmula:C11H21N2O2Pureza:98%Forma y color:SolidPeso molecular:213.29664-Acetamido-2,2,6,6-tetramethylpiperidine 1-oxyl
CAS:4-Acetamido-2,2,6,6-tetramethylpiperidine 1-oxylFórmula:C11H21N2O2Pureza:98%Forma y color: light yellow to orange solidPeso molecular:213.30g/mol4-Acetamido-2,2,6,6-tetramethylpiperidine 1-Oxyl Free Radical [Catalyst for Oxidation]
CAS:Fórmula:C11H21N2O2Pureza:>98.0%(GC)Forma y color:Light yellow to Brown powder to crystalinePeso molecular:213.304-Acetamido-2,2,6,6-tetramethylpiperidine 1-oxyl
CAS:Fórmula:C11H21N2O2Pureza:95.0%Forma y color:SolidPeso molecular:213.164-Acetamido-2,2,6,6-Tetramethylpiperidine-1-Oxyl (Acetamido TEMPO) pure, 97%
CAS:Fórmula:C11H21N2O2Pureza:min. 97%Forma y color:Orange to red to brown to orange- red, Powder, ClearPeso molecular: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.
Fórmula:C11H21N2O2Pureza:Min. 98 Area-%Peso molecular:213.3 g/molRef: 10-F987928
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