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3637-10-3

3637-10-3 Structure

3637-10-3 Structure
IdentificationMore
[Name]

4-HYDROXY-TEMPO
[CAS]

3637-10-3
[Synonyms]

2,2,6,6-TETRAMETHYL-4-HYDROXY-1-PIPERIDINYLOXY
2,2,6,6-TETRAMETHYL-4-PIPERIDINOL 1-OXYL
2,2,6,6-tetramethyl freeagaoxy-4-piperidyl
4-HYDROXY-2,2,6,6-TETRAMETHYL-1-PIPERIDIN-1-YLOXY
4-HYDROXY-2,2,6,6-TETRAMETHYL-1-PIPERIDINYLOXY, FREE RADICAL
4-HYDROXY-2,2,6,6-TETRAMETHYLPIPERIDINE 1-OXYL
4-HYDROXY-2,2,6,6-TETRAMETHYLPIPERIDINE-N-OXYL
4-HYDROXY-2,2,6,6-TETRAMETHYL-PIPERIDINOOXY
4-HYDROXY-2,2,6,6-TETRAMETHYL-PIPERIDINOOXY, FREE RADICAL
4-HYDROXY-2,2,6,6-TETRAMETHYLPIPERIDINYLOXY
4-HYDROXY-2,2,6,6-TETRAMETHYLPIPERIDINYLOXY FREE RADICAL
4-HYDROXY-TEMPO
4-HYDROXY-TEMPO, FREE RADICAL
4-OH-TEMPO
HYDROXY-TEMPO
TEMPOL
1,4-Dihydroxy-2,2,6,6-tetramethylpiperidine
2,2,6,6-tetramethyl-piperidine-1,4-diol
4-Piperidinol, 2,2,6,6-tetramethyl-, 1-oxide
[EINECS(EC#)]

218-761-4
[Molecular Formula]

C9H18NO2 *
[MDL Number]

MFCD00006478
[Molecular Weight]

172.24
[MOL File]

3637-10-3.mol
Chemical PropertiesBack Directory
[Melting point ]

69-71 °C(lit.)
[Boiling point ]

260.2±29.0 °C(Predicted)
[density ]

1.029±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[pka]

14.02±0.70(Predicted)
[InChI]

InChI=1S/C9H19NO2/c1-8(2)5-7(11)6-9(3,4)10(8)12/h7,11-12H,5-6H2,1-4H3
[InChIKey]

CSGAUKGQUCHWDP-UHFFFAOYSA-N
[SMILES]

N1(O)C(C)(C)CC(O)CC1(C)C
[CAS DataBase Reference]

3637-10-3(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

R22:Harmful if swallowed.
R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
[WGK Germany ]

1
[RTECS ]

TN8991000
[TSCA ]

TSCA listed
Hazard InformationBack Directory
[Uses]

2,2,6,6-Tetramethylpiperidine-1,4-diol is related to 4-Hydroxy-2,2,6,6-tetramethyl-1-piperidinyloxy (H956500), which is a free radical scavenger. 2,2,6,6-Tetramethylpiperidine-1,4-diol has also been shown to be an in vitro and in vivo radioprotector. It is used as a reagent in stereoselective preparation of tetrasubstituted triarylated olefins via Pd-catalyzed sequential oxidative Heck arylation of alkenes with arylboronic acids using nitroxides as oxidants.
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