CASNumber2226-96-2
EmpiricalFormula(HillNotation)C9H18NO2
MolecularWeight172.24
BeilsteinRegistryNumber1422990
ECNumber218-760-9
MDLnumberMFCD00006478
PubChemSubstanceID24850555
Popular Documents: FTIR(PDF)
Properties:
RelatedCategories | AnalyticalReagents,Analytical/Chromatography,ChemicalSynthesis,ElectronSpinResonance(ESR/EPR)Spectroscopy,RADIcalChemistry, | ||||||||||
InChIKey | UZFMOKQJFYMBGY-UHFFFAOYSAassay | 97% | composition | Carboncontent,60.6-65.0% | | Nitrogencontent,7.8-8.4% | mp | 69-71 °C(lit.) | storagetemp. | 2-8°C | Description:ApplicationSpinlabelreagentusedinthechatacterizationofantagoNISTandagonistbindingsitesofNK1receptor.Alsousedtomeasurereactiveoxygengenerationinheartmusclebyelectronspinresonancespectroscopy.CellsthatoverexpressCYP2E1canbeprotectedfromarachidonicacidtoxicitydamagebyTEMPOL. 4-Hydroxy-TEMPO(HO-TEMPO)maybeemployedascatalystfortheoxidationofalcoholstothecorrespondingaldehydes.ItmaybeemployedforthepreparationofTEMPObasedpolymercatalystsystems,whichareusefulfortheAnellioxidationofvariousprimaryalcohols.Itmaybeusedasstartingreagentinthesynthesisof4-(2,2,6,6-tetramethyl-1- Afluorous-taggedTEMPOderivativewaspreparedfromthederivedTEMPOpropargylicetherandsubsequent"click"reactionwithafluorousazide.ThisTEMPOderivativeprovedtobeahighlyeffectivecatalystintheoxidationofalcoholswithbleach. SpinlabelforstudyingBIOLOGicalcompoundsandpolymers. 1,5,25ginglassbottle 4-Hydroxy-TEMPOisa4-substituted2,2,6,6-tetramethylpiperi |