503822-44-4

Basic information

• Product Name: (1'R,4R)-4-ethyl-2-(2'-hydroxy-1'-phenylethyl)-1,2,3,4-tetrahydroisoquinoline
• Synonyms: (1'R,4R)-4-ethyl-2-(2'-hydroxy-1'-phenylethyl)-1,2,3,4-tetrahydroisoquinoline
• CAS NO: 503822-44-4
• Molecular Weight: 281.398
• Mol File: 503822-44-4.mol

Chemical Properties

• CAS DataBase Reference: (1'R,4R)-4-ethyl-2-(2'-hydroxy-1'-phenylethyl)-1,2,3,4-tetrahydroisoquinoline(CAS DataBase Reference)
• NIST Chemistry Reference: (1'R,4R)-4-ethyl-2-(2'-hydroxy-1'-phenylethyl)-1,2,3,4-tetrahydroisoquinoline(503822-44-4)
• EPA Substance Registry System: (1'R,4R)-4-ethyl-2-(2'-hydroxy-1'-phenylethyl)-1,2,3,4-tetrahydroisoquinoline(503822-44-4)

Safety Data

• Hazardous Substances Data: 503822-44-4(Hazardous Substances Data)

Upstream product

• 503822-38-6 (3R,6R)-6-ethyl-3-phenyl-2,3,6,10b-tetrahydro-5H-oxazolo[2,3-a]isoquinoline 
• 56613-80-0 D-2-phenylglycinol 
• 503822-32-0 (R)-2-(but-2-enylamino)-2-phenylethanol 
• 503822-35-3 (2R,4R)-2-(2-bromophenyl)-3-(but-2-enyl)-4-phenyl-1,3-oxazolidine 

Downstream Products

• 154140-71-3 (R)-4-ethyl-1,2,3,4-tetrahydroisoquinoline 

Relevant articles and documents

Aryl radical cyclization of chiral 3-allyl-2-(2-bromophenyl)-1,3-oxazolidines with tributyltin hydride

Stereoselective radical cyclization of (4R)-3-allyl-2-(2-bromophenyl)-4-phenyl-1,3-oxazolidine promoted by the initiator/tributyltin hydride system constructed the chiral oxazolo[2,3-a]tetrahydroisoquinoline skeleton. These tricyclic compounds were transf