1241681-13-9

Basic information

• Product Name: (1S,3R)-1-AMINO-1-PHENYLPENTAN-3-OL
• Synonyms: (1S,3R)-1-AMINO-1-PHENYLPENTAN-3-OL;Benzenepropanol, γ-amino-α-ethyl-, (αR,γS)-
• CAS NO: 1241681-13-9
• Molecular Formula: C11H17NO
• Molecular Weight: 179.26
• Mol File: 1241681-13-9.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (1S,3R)-1-AMINO-1-PHENYLPENTAN-3-OL(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,3R)-1-AMINO-1-PHENYLPENTAN-3-OL(1241681-13-9)
• EPA Substance Registry System: (1S,3R)-1-AMINO-1-PHENYLPENTAN-3-OL(1241681-13-9)

Safety Data

• Hazardous Substances Data: 1241681-13-9(Hazardous Substances Data)

Upstream product

• 613-91-2 acetophenone oxime 
• 109787-95-3 1-phenyl-1-oxo-3-hydroxypent-4-ene 
• 92287-44-0 3-phenyl-5-vinyl-4,5-dihydroisoxazole 
• 59239-04-2 1-phenyl-4-penten-1-one oxime 
• 98-86-2 acetophenone 

Relevant articles and documents

Synthesis of 5-Vinyl-2-isoxazolines by Palladium-Catalyzed Intramolecular O-Allylation of Ketoximes

An efficient method for the synthesis of 5-vinyl-2-isoxazolines by Pd-catalyzed intramolecular O-allylation of ketoximes has been developed. The reaction involves Pd(0)-catalyzed π-allyl formation via leaving group ionization or Pd(II)-catalyzed allylic C-H activation followed by intramolecular nucleophilic oxime oxygen attack. This methodology has been elaborated to various value-added products by epoxidation, Wacker oxidation, cross-metathesis, hydroboration-oxidation, dihydroxylation, and catalytic hydrogenation.