4972-13-8

Basic information

• Product Name: 4-Piperidinol, 1-hydroxy-2,2,6,6-tetramethyl-, 4-benzoate
• CAS NO: 4972-13-8
• Molecular Formula: C16H23NO3
• Molecular Weight: 277.364
• Mol File: 4972-13-8.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: 4-Piperidinol, 1-hydroxy-2,2,6,6-tetramethyl-, 4-benzoate(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Piperidinol, 1-hydroxy-2,2,6,6-tetramethyl-, 4-benzoate(4972-13-8)
• EPA Substance Registry System: 4-Piperidinol, 1-hydroxy-2,2,6,6-tetramethyl-, 4-benzoate(4972-13-8)

Safety Data

• Hazardous Substances Data: 4972-13-8(Hazardous Substances Data)

Upstream product

• 3225-26-1 4-(benzyloxycarbonyl)-2,2,6,6-tetramethylpiperidine-1-oxyl 
• 558-17-8 tert-Butyl iodide 
• 108-38-3 m-xylene 
• 74-88-4 methyl iodide 
• 93-46-9 N,N'-di(2-naphthyl)-p-phenylenediamine 
• 101-70-2 bis(4-methoxyphenyl)amine 
• 135-88-6 N-Phenyl-2-naphthylamine 
• 620-93-9 di-p-tolylamine 
• 5650-10-2 N-phenyl-(4-isopropyl)aniline 

Downstream Products

• 131840-68-1 diethyl 2-(4-benzoyloxy-2,2,6,6-tetramethylpiperidin-1-oxy)ethylphosphonate 
• 1234306-07-0 benzoic acid 1-(N,N'-dicyclohexyl-carbamimidoyloxy)-2,2,6,6-tetramethyl-piperidin-4-yl ester 
• 1234306-09-2 benzoic acid 1-(N,N'-di-p-tolyl-carbamimidoyloxy)-2,2,6,6-tetramethyl-piperidin-4-yl ester 
• 376587-87-0 1-tert-Butoxycarbonyloxy-2,2,6,6-tetramethylpiperidin-4-yl Benzoate 
• 376587-88-1 1-Diphenylphosphinoyloxy-2,2,6,6-tetramethylpiperidin-4-yl Benzoate 
• 7031-92-7 1,4-dibenzoyloxy-2,2,6,6-tetramethylpiperidine 
• 376587-81-4 1-(2,2-Dimethylpropionyloxy)-2,2,6,6-tetramethylpiperidin-4-yl benzoate 

Relevant articles and documents

Eclipsed ground-state conformations of the tert-butyl-X bond in N-tert-butoxy- and N-neopentyl-2,2,6,6-tetramethylpiperidine. X-ray crystal structure determinations and molecular mechanics calculations

X-ray crystallographic studies of derivatives of N-methoxy- and N-tert-butoxy-2,2,6,6-tetramethylpiperidine show that as expected the N-O bond is staggered with respect to the C-H bonds of the methoxy group in the former case, yet it eclipses a C-methyl b

The thermal reaction of sterically hindered nitroxyl radicals with allylic and benzylic substrates: Experimental and computational evidence for divergent mechanisms

The reaction of stable sterically hindered nitroxyl radicals with benzylic and allylic substrates was investigated. An allyloxyamine derivative was obtained by the reaction of 2 molar equiv of a nitroxyl radical with an unactivated alkene. Experimental an

Prevention of oxidation in petrochemical extraction solvents

A wide variety of hindered amine compounds are effective as antioxidant stabilizers to prevent the oxidation of liquid hydrocarbons and of oxygenated compounds, such as sulfolane or tetraethylene glycol, used as extraction solvents in the petroleum industry.