198494-12-1

Basic information

• Product Name: Acetic acid 1'-acetoxy-4,4'-bis-(3-acetylamino-phenyl)-8,8'-dimethoxy-6,6'-dimethyl-[2,2']binaphthalenyl-1-yl ester
• Synonyms: Acetic acid 1'-acetoxy-4,4'-bis-(3-acetylamino-phenyl)-8,8'-dimethoxy-6,6'-dimethyl-[2,2']binaphthalenyl-1-yl ester
• CAS NO: 198494-12-1
• Molecular Weight: 724.81
• Mol File: 198494-12-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Acetic acid 1'-acetoxy-4,4'-bis-(3-acetylamino-phenyl)-8,8'-dimethoxy-6,6'-dimethyl-[2,2']binaphthalenyl-1-yl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Acetic acid 1'-acetoxy-4,4'-bis-(3-acetylamino-phenyl)-8,8'-dimethoxy-6,6'-dimethyl-[2,2']binaphthalenyl-1-yl ester(198494-12-1)
• EPA Substance Registry System: Acetic acid 1'-acetoxy-4,4'-bis-(3-acetylamino-phenyl)-8,8'-dimethoxy-6,6'-dimethyl-[2,2']binaphthalenyl-1-yl ester(198494-12-1)

Safety Data

• Hazardous Substances Data: 198494-12-1(Hazardous Substances Data)

Upstream product

• 78887-39-5 3-Acetamidophenylboronic acid 
• 160466-00-2 Acetic acid 1'-acetoxy-8,8'-dimethoxy-6,6'-dimethyl-4,4'-bis-trifluoromethanesulfonyloxy-[2,2']binaphthalenyl-1-yl ester 
• 106-51-4 p-benzoquinone 
• 160465-99-6 Acetic acid 4,1',4'-triacetoxy-8,8'-dimethoxy-6,6'-dimethyl-[2,2']binaphthalenyl-1-yl ester 
• 160466-04-6 Acetic acid 1'-acetoxy-4,4'-dihydroxy-8,8'-dimethoxy-6,6'-dimethyl-[2,2']binaphthalenyl-1-yl ester 
• 75445-89-5 4,4',8,8'-Tetramethoxy-6,6'-dimethyl-2,2'-binaphthyliden-1,1'-dion 
• 178949-51-4 5-Methoxy-7-methyl-naphthalene-1,4-diol 
• 76927-59-8 (E)-((1-methoxy-3-methylbuta-1,3-dien-1-yl)oxy)trimethylsilane 
• 34555-32-3 4,8-dimethoxy-6-methylnaphth-1-ol 
• 65565-56-2 5-methoxy-7-methylnaphthalene-1,4-dione 
• 17734-94-0 Mamegakinon-dimethylether 

Relevant articles and documents

Structural analogues of the michellamine anti-HIV agents. Importance of the tetrahydroisoquinoline rings for biological activity

A series of michellamine structural analogues was prepared in which the tetrahydroisoquinoline rings were substituted with a variety of simple aromatic ring systems. Additionally, the methyl groups on the central bis-naphthalene cores were replaced with hydrogen and methoxy. All the analogues were devoid of anti-HIV activity, suggesting that the heterocyclic portion of the tetrahydroisoquinoline ring is crucial for biological activity.