26648-71-5

Basic information

• Product Name: (R)-1-[(2R)-2β-Piperidinyl]-2-pentanol
• Synonyms: (-)-Halosaline;(2R)-1-[(2R)-2-Piperidinyl]-2-pentanol;(R)-1-[(2R)-2β-Piperidinyl]-2-pentanol;(αR,2R)-α-Propyl-2-piperidineethanol;Halosaline
• CAS NO: 26648-71-5
• Molecular Formula: C10H21 N O
• Molecular Weight: 171.28
• Mol File: 26648-71-5.mol
• Article Data: 10

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (R)-1-[(2R)-2β-Piperidinyl]-2-pentanol(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-1-[(2R)-2β-Piperidinyl]-2-pentanol(26648-71-5)
• EPA Substance Registry System: (R)-1-[(2R)-2β-Piperidinyl]-2-pentanol(26648-71-5)

Safety Data

• Hazardous Substances Data: 26648-71-5(Hazardous Substances Data)

Usage

Uses

(-)-Halosaline is a molecule of interest because of its memory enhancing properties.

Upstream product

• 190383-62-1 [2R-(2R)]-1-benzyloxycarbonyl-2-(2-hydroxy-4-pentenyl)piperidine 
• 245092-73-3 1-[1-(toluene-4-sulfonyl)piperidin-2-yl]pentan-2-ol 
• 756821-41-7 (2R,2'R)-1-(1',2',3',6'-tetrahydropyridin-2'-yl)pent-4-en-2-ol 
• 945773-00-2 (R)-6-((R)-2-hydroxypentyl)piperidin-2-one 
• 945772-75-8 C₁₀H₁₇IO₂ 
• 945772-98-5 C₁₀H₁₇N₃O₂ 
• 139406-51-2 (R)-2-propylethylene oxide 
• 756821-40-6 (2R,2'R)-1-[1'-(toluene-4-sulfonyl)-1',2',3',6'-tetrahydropyridin-2'-yl]pent-4-en-2-ol 
• 756821-38-2 (1R,6R)-acetic acid 6-(N-p-toluenesulfonylamino)cyclohept-3-enyl ester 
• 756821-35-9 (1R,6R)-acetic acid 6-(N-allyl-N-p-toluenesulfonylamino)cyclohept-3-enyl ester 
• 756821-39-3 (1R,2'R)-acetic acid 1-[1'-(toluene-4-sulfonyl)-1',2',3',6'-tetrahydropyridin-2'-ylmethyl]but-3-enyl ester 
• 756821-37-1 (1R,6R)-N-(tert-butoxycarbonyl)-N-[(6-tert-butyldimethylsilanyloxy)cyclohept-3-enyl]toluensulfonamide 
• 190383-57-4 [2R-(2S)]-1-benzyloxycarbonyl-2-(2,3-epoxypropyl)piperidine 
• 60410-16-4 (1R,4S)-4-hydroxy-2-cyclopentene-1-yl acetate 

Relevant articles and documents

Organocatalytic stereoselective approach to the total synthesis of (-)-halosaline

A practical and efficient organocatalytic approach to the synthesis of substituted piperidine alkaloids in high enantio- and diastereomeric excess was achieved using proline-catalyzed sequential α-aminoxylation/α- amination reaction and HWE olefination reaction of an aldehyde.

Stereoselective synthesis of anti-1,3-aminoalcohols via reductive opening of 4-amidotetrahydropyrans derived from the Prins/Ritter sequence

A novel method has been devised for anti-1,3-aminoalcohols through reductive elimination of iodomethyltetrahydropyrans which are in turn derived from a Prins/Ritter reaction sequence. The synthetic versatility of this method has been explored in the total

Cyclopentanone ring expansion leading to functionalized δ-lactams: Short synthesis of simple sedum alkaloids

Equation Presented Monosubstituted epoxides react with (cyclopentenyloxy) trimethylsilane to afford, after subsequent oxidative fragmentation, a pair of diastereomeric 8-membered iodolactones. When these lactones are separately treated with sodium azide,