1360538-03-9

Basic information

• Product Name: ((1S,4R)-4-(6-(cyclopropylamino)-2-((4-methoxybenzyl)amino)-9H-purin-9-yl)cyclopent-2-en-1-yl)methanol
• Synonyms: ((1S,4R)-4-(6-(cyclopropylamino)-2-((4-methoxybenzyl)amino)-9H-purin-9-yl)cyclopent-2-en-1-yl)methanol
• CAS NO: 1360538-03-9
• Molecular Weight: 406.487
• Mol File: 1360538-03-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: ((1S,4R)-4-(6-(cyclopropylamino)-2-((4-methoxybenzyl)amino)-9H-purin-9-yl)cyclopent-2-en-1-yl)methanol(CAS DataBase Reference)
• NIST Chemistry Reference: ((1S,4R)-4-(6-(cyclopropylamino)-2-((4-methoxybenzyl)amino)-9H-purin-9-yl)cyclopent-2-en-1-yl)methanol(1360538-03-9)
• EPA Substance Registry System: ((1S,4R)-4-(6-(cyclopropylamino)-2-((4-methoxybenzyl)amino)-9H-purin-9-yl)cyclopent-2-en-1-yl)methanol(1360538-03-9)

Safety Data

• Hazardous Substances Data: 1360538-03-9(Hazardous Substances Data)

Upstream product

• 146864-12-2 (1S,5R)-6-azabicyclo[3.2.0]hept-3-en-7-one 
• 268737-87-7 ((1S,4R)-4-(2,6-dichloro-9H-purin-9-yl)cyclopent-2-en-1-yl)methanol 
• 5451-40-1 2,6 dichloropurine 
• 97911-48-3 (+/-)-6-azabicyclo[3.2.0]hept-3-en-7-one 
• 1108600-43-6 (1S,5R)-6-tosyl-6-azabicyclo[3.2.0]hept-3-en-7-one 
• 1108600-46-9 ((1S,4R)-4-(2-chloro-6-(cyclopropylamino)-9H-purin-9-yl)cyclopent-2-en-1-yl)methanol 
• 2393-23-9 4-methoxy-benzylamine 
• 1108600-45-8 (1S,4R)-4-(2,6-dichloro-9H-purin-9-yl)-N-methyl-N-tosylcyclopent-2-enecarboxamide 
• 1108600-44-7 (1S,4R)-4-(2,6-dichloro-9H-purin-9-yl)-N-tosylcyclopent-2-enecarboxamide 
• 1108600-48-1 tetrabutylammonium 2,6-dichloropurin-9-ide 

Downstream Products

• 136470-78-5 abacavir 

Relevant articles and documents

Enantioselective synthesis of the carbocyclic nucleoside (-)-abacavir

An enantiopure β-lactam with a suitably disposed electron withdrawing group on nitrogen, participated in a π-allylpalladium mediated reaction with 2,6-dichloropurine tetrabutylammonium salt to afford an advanced cis-1,4-substituted cyclopentenoid with both high regio- and stereoselectivity. This advanced intermediate was successfully manipulated to the total synthesis of (-)-Abacavir.