1377322-04-7

Basic information

• Product Name: (+)-(Z,2'S,3R,4aR,7S)-7-[2'-(benzyloxy)heptyl]-2-(4-methoxybenzyl)-3-(pent-2-en-1-yl)hexahydropyrrolo[1,2-c]pyrimidin-1(2H)-one
• Synonyms: (+)-(Z,2'S,3R,4aR,7S)-7-[2'-(benzyloxy)heptyl]-2-(4-methoxybenzyl)-3-(pent-2-en-1-yl)hexahydropyrrolo[1,2-c]pyrimidin-1(2H)-one
• CAS NO: 1377322-04-7
• Molecular Weight: 532.767
• Mol File: 1377322-04-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (+)-(Z,2'S,3R,4aR,7S)-7-[2'-(benzyloxy)heptyl]-2-(4-methoxybenzyl)-3-(pent-2-en-1-yl)hexahydropyrrolo[1,2-c]pyrimidin-1(2H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: (+)-(Z,2'S,3R,4aR,7S)-7-[2'-(benzyloxy)heptyl]-2-(4-methoxybenzyl)-3-(pent-2-en-1-yl)hexahydropyrrolo[1,2-c]pyrimidin-1(2H)-one(1377322-04-7)
• EPA Substance Registry System: (+)-(Z,2'S,3R,4aR,7S)-7-[2'-(benzyloxy)heptyl]-2-(4-methoxybenzyl)-3-(pent-2-en-1-yl)hexahydropyrrolo[1,2-c]pyrimidin-1(2H)-one(1377322-04-7)

Safety Data

• Hazardous Substances Data: 1377322-04-7(Hazardous Substances Data)

Upstream product

• 2100-17-6 4-pentenal 
• 31849-78-2 (Z)-1-bromo-1-butene 
• 1377322-03-6 (+)-(2R,2'S,5S)-2-allyl-5-[2'-(benzyloxy)heptyl]-N-(4-methoxybenzyl)pyrrolidine-1-carboxamide 
• 1377322-02-5 (+)-(E,2S,2'S,5R)-tert-butyl 2-[2'-(benzyloxy)heptyl]-5-[3-(trimethylsilyl)allyl]pyrrolidine-1-carboxylate 
• 1377322-01-4 (+)-(5S,7S)-tert-butyl 7-(benzyloxy)dodec-1-en-5-ylcarbamate 
• 1377322-08-1 (+)-(Ss,5S,7S)-N-[7-(benzyloxy)dodec-1-en-5-yl]-2-methylpropane-2-sulfinamide 
• 1377322-00-3 (+)-(Ss,5S,7S)-N-(7-hydroxydodec-1-en-5-yl)-2-methylpropane-2-sulfinamide 
• 1377321-99-7 (+)-(Ss,5S)-2-methyl-N-(7-oxododec-1-en-5-yl)propane-2-sulfinamide 

Downstream Products

• 1377322-06-9 (+)-(Z,2'S,3R,4aR,7S)-7-[2'-(benzyloxy)heptyl]-2-(4-methoxybenzyl)-3-(pent-2-en-1-yl)hexahydropyrrolo[1,2-c]pyrimidin-1(2H)-iminium tetrafluoroborate 

Relevant articles and documents

Asymmetric total synthesis of (+)-merobatzelladine B

Putting the syn in synthesis: The first total synthesis of (+)-merobatzelladineB was accomplished using an iterative sequence of stereoselective palladium-catalyzed alkene carboamination reactions for formation of two of the three rings. This represents a new strategy for the generation of polycyclic guanidine natural products, and provides access to compounds with a synrelationship between the C6 hydrogen atom and the C8 alkyl group. Copyright