297741-05-0

Basic information

• Product Name: (S)-1-[4-(2-hydroxyethyl)phenoxy]-2,3-epoxypropane
• Synonyms: (S)-1-[4-(2-hydroxyethyl)phenoxy]-2,3-epoxypropane
• CAS NO: 297741-05-0
• Molecular Weight: 194.23
• Mol File: 297741-05-0.mol

Chemical Properties

• CAS DataBase Reference: (S)-1-[4-(2-hydroxyethyl)phenoxy]-2,3-epoxypropane(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-1-[4-(2-hydroxyethyl)phenoxy]-2,3-epoxypropane(297741-05-0)
• EPA Substance Registry System: (S)-1-[4-(2-hydroxyethyl)phenoxy]-2,3-epoxypropane(297741-05-0)

Safety Data

• Hazardous Substances Data: 297741-05-0(Hazardous Substances Data)

Upstream product

• 104857-48-9 1-[4-(2-hydroxyethyl)phenoxy]-2,3-epoxypropane 
• 501-94-0 p-hydroxyphenethyl alcohol 
• 51594-55-9 (R)-(-)-epichlorohydrin 

Downstream Products

• 131564-69-7 (-)-O-Demethylmetoprolol 
• 947340-61-6 (5S)-2-(4-((3-isopropyl-2-phenyloxazolidin)-5-methoxy)phenyl)-4-ethanol 
• 104857-50-3 (5S)-5-(4-((2-cyclopropylmethoxy)ethyl)phenoxy)methyl-3-isopropyl-2-phenyloxazolidine 
• 93221-48-8 (-)-Betaxolol 
• 81024-42-2 S-(-)-metoprolol 
• 929205-75-4 (R)-1-iodo-3-[4-(2-methoxy ethyl)phenoxy]propan-2-ol 
• 874809-42-4 (S)-2-[4-(2-cyclopropylmethoxy ethyl)phenoxymethyl]oxirane 

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,

Concise synthesis of β-blockers (S)-metoprolol and (S)-betaxolol using hydrolytic kinetic resolution

Enantiopure (S)-metoprolol and (S)-betaxolol were prepared in an extremely simple and practical way using Jacobsen's hydrolytic kinetic resolution of terminal epoxides in isopropanol.