160516-03-0

Basic information

• Product Name: 9-benzyl-6-(α-ethoxyvinyl)purine
• Synonyms: 9-benzyl-6-(α-ethoxyvinyl)purine
• CAS NO: 160516-03-0
• Molecular Weight: 280.329
• Mol File: 160516-03-0.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 9-benzyl-6-(α-ethoxyvinyl)purine(CAS DataBase Reference)
• NIST Chemistry Reference: 9-benzyl-6-(α-ethoxyvinyl)purine(160516-03-0)
• EPA Substance Registry System: 9-benzyl-6-(α-ethoxyvinyl)purine(160516-03-0)

Safety Data

• Hazardous Substances Data: 160516-03-0(Hazardous Substances Data)

Upstream product

• 100-39-0 benzyl bromide 
• 4261-14-7 9-benzyl-9H-purin-6-ylamine 
• 87-42-3 6-chloropurine 
• 100-44-7 benzyl chloride 
• 97674-02-7 tributyl(1-ethoxyvinyl)stannane 
• 83135-13-1 9-benzyl-6-iodo-9H-purine 
• 1928-76-3 9-benzyl-6-chloro-9H-purine 

Downstream Products

• 958867-87-3 methyl-4-(9-benzyl-9H-purin-6-yl)-2-hydroxy-4-oxobut-2-enoate 
• 160516-12-1 6-acetyl-9-benzylpurine 

Relevant articles and documents

DIKETO ACIDS WITH NUCLEOBASE SCAFFOLDS: ANTI-HIV REPLICATION INHIBITORS TARGETED AT HIV INTEGRASE IN COMBINATION THERAPY

A new class of diketo acids constructed on nucleobase scaffolds, designed as inhibitors of HIV replication through inhibition of HIV integrase, is described. These compounds are useful in the prevention or treatment of infection by HFV and in the treatmen

Diketo acids with nucleobase scaffolds: anti-HIV replication inhibitors targeted at HIV integrase

A new class of diketo acids constructed on nucleobase scaffolds, designed as inhibitors of HIV replication through inhibition of HIV integrase, is described. These compounds are useful in the prevention or treatment of infection by HIV and in the treatmen

6-Halopurines in palladium-catalyzed coupling with organotin and organozinc reagents

N-9 and N-7 benzylated 6-halopurines readily participate in palladium catalyzed cross coupling reactions with organotin and organozinc derivatives. In most instances the 6-chloropurines can be used. Organostannanes are excellent reagents for the introduction of alkenyl and aryl substituents, but organozinc compounds are the reagents of choice for the introduction of alkyl groups.