1602588-73-7

Basic information

• Product Name: (+/-)-2-(3-acetylbenzyl)-7-methoxy-3-methyl-6-(triisopropylsilyloxy)-1,2,3,4-tetrahydroisoquinoline
• Synonyms: (+/-)-2-(3-acetylbenzyl)-7-methoxy-3-methyl-6-(triisopropylsilyloxy)-1,2,3,4-tetrahydroisoquinoline
• CAS NO: 1602588-73-7
• Molecular Weight: 481.751
• Mol File: 1602588-73-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (+/-)-2-(3-acetylbenzyl)-7-methoxy-3-methyl-6-(triisopropylsilyloxy)-1,2,3,4-tetrahydroisoquinoline(CAS DataBase Reference)
• NIST Chemistry Reference: (+/-)-2-(3-acetylbenzyl)-7-methoxy-3-methyl-6-(triisopropylsilyloxy)-1,2,3,4-tetrahydroisoquinoline(1602588-73-7)
• EPA Substance Registry System: (+/-)-2-(3-acetylbenzyl)-7-methoxy-3-methyl-6-(triisopropylsilyloxy)-1,2,3,4-tetrahydroisoquinoline(1602588-73-7)

Safety Data

• Hazardous Substances Data: 1602588-73-7(Hazardous Substances Data)

Upstream product

• 1064202-09-0 (+/-)-2-acetyl-6-benzyloxy-7-methoxy-3-methyl-1,2,3,4-tetrahydroisoquinoline 
• 35645-86-4 (+/-)-N-(1-(3-benzyloxy-4-methoxyphenyl)propan-2-yl)acetamide 
• 60011-91-8 (+/-)-1-(3-benzyloxy-4-methoxyphenyl)propan-2-amine 
• 321125-47-7 (+/-)-2-benzyloxy-1-methoxy-4-(2-nitropropyl)benzene 
• 1064202-02-3 2-benzyloxy-1-methoxy-4-((E)-2-nitroprop-1-enyl)benzene 
• 1602588-43-1 (+/-)-7-methoxy-3-methyl-6-(triisopropylsilyloxy)-1,2,3,4-tetrahydro-isoquinoline 
• 75369-41-4 1-[3-(bromomethyl)phenyl]ethan-1-one 
• 1602588-46-4 (+/-)-6-hydroxy-7-methoxy-3-methyl-1,2,3,4-tetrahydroisoquinoline 
• 6346-05-0 3-benzyloxy-4-methoxybenzaldehyde 
• 1064202-11-4 (+/-)-6-benzyloxy-7-methoxy-3-methyl-1,2,3,4-tetrahydroisoquinoline 

Downstream Products

• 1602588-96-4 (+/-)-2-(3-acetylbenzyl)-6-hydroxy-7-methoxy-3-methyl-1,2,3,4-tetrahydroisoquinoline 
• 1602589-23-0 (+/-)-2-(3-acetylbenzyl)-7-methoxy-3-methyl-6-sulfamoyloxy-1,2,3,4-tetrahydroisoquinoline 

Relevant articles and documents

Synthesis, antitubulin, and antiproliferative sar of c3/c1-substituted tetrahydroisoquinolines

The syntheses and antiproliferative activities of novel substituted tetrahydroisoquinoline derivatives and their sulfamates are discussed. Biasing of conformational populations through substitution on the tetrahydroisoquinoline core at C1 and C3 has a pro