1379615-12-9

Basic information

• Product Name: methyl (1S,2S,3R,10bR)-8,9-dimethoxy-2-(4-methoxyphenyl)-1-[(E)-2-methoxyvinyl]-3-methyl-1,2,3,5,6,10b-hexahydropyrrolo[2,1-a]isoquinoline-3-carboxylate
• Synonyms: methyl (1S,2S,3R,10bR)-8,9-dimethoxy-2-(4-methoxyphenyl)-1-[(E)-2-methoxyvinyl]-3-methyl-1,2,3,5,6,10b-hexahydropyrrolo[2,1-a]isoquinoline-3-carboxylate
• CAS NO: 1379615-12-9
• Molecular Weight: 467.562
• Mol File: 1379615-12-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: methyl (1S,2S,3R,10bR)-8,9-dimethoxy-2-(4-methoxyphenyl)-1-[(E)-2-methoxyvinyl]-3-methyl-1,2,3,5,6,10b-hexahydropyrrolo[2,1-a]isoquinoline-3-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl (1S,2S,3R,10bR)-8,9-dimethoxy-2-(4-methoxyphenyl)-1-[(E)-2-methoxyvinyl]-3-methyl-1,2,3,5,6,10b-hexahydropyrrolo[2,1-a]isoquinoline-3-carboxylate(1379615-12-9)
• EPA Substance Registry System: methyl (1S,2S,3R,10bR)-8,9-dimethoxy-2-(4-methoxyphenyl)-1-[(E)-2-methoxyvinyl]-3-methyl-1,2,3,5,6,10b-hexahydropyrrolo[2,1-a]isoquinoline-3-carboxylate(1379615-12-9)

Safety Data

• Hazardous Substances Data: 1379615-12-9(Hazardous Substances Data)

Upstream product

• 20232-39-7 3,4-dihydro-6,7-dimethoxyisoquinoline hydrochloride 
• 1963-36-6 4-methoxycinnamaldehyde 
• 1379615-05-0 methyl (1R,2S,3R,10bR)-1-formyl-8,9-dimethoxy-2-(4-methoxyphenyl)-3-methyl-1,2,3,5,6,10b-hexahydropyrrolo[2,1-a]isoquinoline-3-carboxylate 
• 4009-98-7 (methoxymethyl)triphenylphosphonium chloride 

Downstream Products

• 1379615-09-4 methyl (1R,2S,3R,10bR)-8,9-dimethoxy-2-(4-methoxyphenyl)-3-methyl-1-(2-oxoethyl)-1,2,3,5,6,10b-hexahydropyrrolo[2,1-a]isoquinoline-3-carboxylate 
• 1379615-10-7 methyl (1R,2S,3R,10bR)-1-[(E)-4-ethoxy-4-oxobut-2-en-1-yl]-8,9-dimethoxy-2-(4-methoxyphenyl)-3-methyl-1,2,3,5,6,10b-hexahydropyrrolo[2,1-a]isoquinoline-3-carboxylate 

Relevant articles and documents

Asymmetric synthesis of hexahydropyrrolo-isoquinolines by an organocatalytic three-component reaction

Merging three in one by a three-component organocatalytic asymmetric reaction of imines and α-bromoesters or ketones with α,β- unsaturated aldehydes provides optically active pyrrolo-isoquinolines-an important class of molecules in life science. The reaction proceeds with excellent enantioselectivity and a number of transformations of the products obtained demonstrated the potential of the new reaction. Copyright