127983-45-3

Basic information

• Product Name: 6-(2'-hydroxy-2'-phenylethyl)-2,3,4,5-tetrahydropyridine
• CAS NO: 127983-45-3
• Molecular Weight: 219.283
• Mol File: 127983-45-3.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 6-(2'-hydroxy-2'-phenylethyl)-2,3,4,5-tetrahydropyridine(CAS DataBase Reference)
• NIST Chemistry Reference: 6-(2'-hydroxy-2'-phenylethyl)-2,3,4,5-tetrahydropyridine(127983-45-3)
• EPA Substance Registry System: 6-(2'-hydroxy-2'-phenylethyl)-2,3,4,5-tetrahydropyridine(127983-45-3)

Safety Data

• Hazardous Substances Data: 127983-45-3(Hazardous Substances Data)

Upstream product

• 142749-20-0 (R)-2-((S)-2-Hydroxy-2-phenyl-ethyl)-piperidin-1-ol 
• 34418-91-2 2,3,4,5-tetrahydropyridine N-oxide 
• 4801-58-5 N-hydroxypiperidine 
• 105147-78-2 (S)-2-((R)-1-Oxy-2,3,4,5-tetrahydro-pyridin-2-yl)-1-phenyl-ethanol 
• 70546-85-9 2-phenyl-3,3a,4,5,6,7-hexahydro-2H-isoxazolo<2,3-a>pyridine 
• 495-47-6 2-(2'-hydroxy-2'-phenylethyl)piperidine 
• 100-42-5 styrene 

Downstream Products

• 127983-46-4 cis-6-methyl-8-phenyl-9-oxa-1-azabicyclo<4.3.0>nonane 
• 105147-78-2 (S)-2-((R)-1-Oxy-2,3,4,5-tetrahydro-pyridin-2-yl)-1-phenyl-ethanol 
• 131697-74-0 (2S,3aR)-8-Benzyl-3a-methyl-2-phenyl-hexahydro-isoxazolo[2,3-a]pyridin-8-ium; bromide 

Relevant articles and documents

Synthesis and Cycloaddition of 6-Substituted-3,4,5,6-tetrahydropyridine 1-oxides

A study of the regiochemical behaviour of the peracid induced ring opening of several hexahydro-2H-isoxazolopyridines (4), leading mainly to ketonitrones (6), has been carried out.Mercury(II) oxide oxidation of unsymmetrical N-hydroxypiperidines (1

Nitrone Cycloaddition: Peracid Oxidation of Perhydro-1,2-oxazolooxazines

Regiochemistry of peracid induced ring opening of perhydro-1,2-oxazolooxazines (2) and (6) in aprotic solvent is dictated by orientation of lone pair of electrons on nitrogen.In contrast to the case with the corresponding hexahydro-2H-isoxazol

Nitrone Cycloadditions: Synthesis of (+/-)-Andrachamine

The usefulness of the cycloaddition of alkenes to 2-alkyl-2,3,4,5-tetrahydropyridine oxides for the preparation of trans-2,6-dialkylpiperidines is confirmed by a stereoselective synthesis of (+/-)-andrachamine.Peroxy acid oxidation of 9-oxa-1-azabicyclononanes does not lead regioselectively to the corresponding 2-alkyl-2,3,4,5-tetrahydropyridine oxide, as had previously been claimed.