233272-34-9

Basic information

• Product Name: (S)-(+)-7-nitro-N-benzyloxycarbonyl-3-methoxycarbonyl-1,2,3,4-tetrahydroisoquinoline
• Synonyms: (S)-(+)-7-nitro-N-benzyloxycarbonyl-3-methoxycarbonyl-1,2,3,4-tetrahydroisoquinoline
• CAS NO: 233272-34-9
• Molecular Weight: 370.362
• Mol File: 233272-34-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (S)-(+)-7-nitro-N-benzyloxycarbonyl-3-methoxycarbonyl-1,2,3,4-tetrahydroisoquinoline(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-(+)-7-nitro-N-benzyloxycarbonyl-3-methoxycarbonyl-1,2,3,4-tetrahydroisoquinoline(233272-34-9)
• EPA Substance Registry System: (S)-(+)-7-nitro-N-benzyloxycarbonyl-3-methoxycarbonyl-1,2,3,4-tetrahydroisoquinoline(233272-34-9)

Safety Data

• Hazardous Substances Data: 233272-34-9(Hazardous Substances Data)

Upstream product

• 1255720-00-3 C₁₉H₁₉ClN₂O₆ 
• 1255719-98-2 C₁₉H₂₀N₂O₇ 
• 293737-33-4 (S)-methyl 7-nitro-1,2,3,4-tetrahydroisoquinoline-3-carboxylate 
• 501-53-1 benzyl chloroformate 
• 74163-81-8 L-Tic-OH 
• 74-88-4 methyl iodide 

Relevant articles and documents

Enantioselective synthesis of constrained phenylalanine analogues

Constrained phenylalanine derivatives containing hydrophobic groups and hydrogen bond acceptor and/or donor functionalities were synthesized through a tandem palladium-mediated Heck reaction followed by a rhodium(II)-catalyzed asymmetric hydrogenation. Ar

TETRAHYDROISOQUINOLINE COMPOUND AND MEDICINAL USE THEREOF

The present invention provide a tetrahydroisoquinoline compound having a superior ACAT-inhibitory activity and/or anti-oxidation action, particularly, novel compound represented by the formula (I) (wherein each symbol is as described in the specification) and a pharmaceutically acceptable salt thereof.