947340-61-6

Basic information

• Product Name: (5S)-2-(4-((3-isopropyl-2-phenyloxazolidin)-5-methoxy)phenyl)-4-ethanol
• CAS NO: 947340-61-6
• Molecular Weight: 341.45
• Mol File: 947340-61-6.mol

Chemical Properties

• CAS DataBase Reference: (5S)-2-(4-((3-isopropyl-2-phenyloxazolidin)-5-methoxy)phenyl)-4-ethanol(CAS DataBase Reference)
• NIST Chemistry Reference: (5S)-2-(4-((3-isopropyl-2-phenyloxazolidin)-5-methoxy)phenyl)-4-ethanol(947340-61-6)
• EPA Substance Registry System: (5S)-2-(4-((3-isopropyl-2-phenyloxazolidin)-5-methoxy)phenyl)-4-ethanol(947340-61-6)

Safety Data

• Hazardous Substances Data: 947340-61-6(Hazardous Substances Data)

Upstream product

• 959279-50-6 C₂₀H₂₉NO₆ 
• 1312687-84-5 C₁₈H₂₇NO₅ 
• 131564-69-7 (-)-O-Demethylmetoprolol 
• 100-52-7 benzaldehyde 
• 501-94-0 p-hydroxyphenethyl alcohol 
• 104857-48-9 1-[4-(2-hydroxyethyl)phenoxy]-2,3-epoxypropane 
• 62572-94-5 (+/-)-O-Demethylmetoprolol 
• 297741-05-0 (S)-1-[4-(2-hydroxyethyl)phenoxy]-2,3-epoxypropane 
• 100-47-0 benzonitrile 

Downstream Products

• 93221-48-8 (-)-Betaxolol 

Relevant articles and documents

Technique for synthesizing levorotatory betaxolol hydrochloride (by machine translation)

The invention discloses a technique for synthesizing levorotatory betaxolol hydrochloride, the process adopts to hydroxy phenylacetic alcohol and R- epoxy halogen propane is used as starting material, under certain conditions after alkylation, amination,

Chemoenzymatic route to S-betaxolol

An efficient chemoenzymatic route to S-betaxolol is reported. A strain (Rhodotorula mucilaginosa DQ832198) screened from soil was used as biocatalyst for the kinetic resolution of the key acetylated intermediates. Excellent enantiomeric excess (ee99%) was