50347-53-0

Basic information

• Product Name: 5,6-Dihydro-9,10,14-trimethoxy-8H-1,3-dioxolo[4,5-h]isoindolo[1,2-b][3]benzazepin-8-one
• Synonyms: 5,6-Dihydro-9,10,14-trimethoxy-8H-1,3-dioxolo[4,5-h]isoindolo[1,2-b][3]benzazepin-8-one
• CAS NO: 50347-53-0
• Molecular Formula: C₂₁H₁₉NO₆
• Molecular Weight: 381.38
• Mol File: 50347-53-0.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 5,6-Dihydro-9,10,14-trimethoxy-8H-1,3-dioxolo[4,5-h]isoindolo[1,2-b][3]benzazepin-8-one(CAS DataBase Reference)
• NIST Chemistry Reference: 5,6-Dihydro-9,10,14-trimethoxy-8H-1,3-dioxolo[4,5-h]isoindolo[1,2-b][3]benzazepin-8-one(50347-53-0)
• EPA Substance Registry System: 5,6-Dihydro-9,10,14-trimethoxy-8H-1,3-dioxolo[4,5-h]isoindolo[1,2-b][3]benzazepin-8-one(50347-53-0)

Safety Data

• Hazardous Substances Data: 50347-53-0(Hazardous Substances Data)

Upstream product

• 55968-78-0 {2-[6-((Z)-4,5-dimethoxy-3-oxo-2,3-dihydro-isoindol-1-ylidenemethyl)-7-methoxy-benzo[1,3]dioxol-5-yl]-ethyl}-trimethyl-ammonium; iodide 
• 50347-55-2 9,10,14-trimethoxy-5,8,12b,13-tetrahydro-6H-[1,3]dioxolo[4'',5'':4',5']benzo[1',2':4,5]azepino[2,1-a]isoindole 
• 55968-81-5 6,7-dimethoxy-3-((E)-4-methoxy-6-vinyl-benzo[1,3]dioxol-5-ylmethylene)-2,3-dihydro-isoindol-1-one 
• 55968-80-4 narceone imide 
• 55968-77-9 (Z)-Narceine imide 
• 50347-54-1 9,10,14-trimethoxy-5,6,12b,13-tetrahydro-[1,3]dioxolo[4'',5'':4',5']benzo[1',2':4,5]azepino[2,1-a]isoindol-8-one 

Downstream Products

• 50347-54-1 9,10,14-trimethoxy-5,6,12b,13-tetrahydro-[1,3]dioxolo[4'',5'':4',5']benzo[1',2':4,5]azepino[2,1-a]isoindol-8-one 
• 88750-55-4 4-benzyloxy-3,12-dimethoxy-10,11-methylenedioxy-7,8-dihydro-5H-isoindolo-<1,2-b>-<3>-benzazepin-5-one 
• 112496-54-5 C₂₇H₂₃NO₈S 

Relevant articles and documents

REACTION OF DIMETHYLAMINOETHYL DERIVATIVES OF 1-BENZYLIDENISOINDOLIN-3-ONE WITH EPOXIDES

Derivatives of 1-(2-(2-dimethylaminoethyl)benzyliden)isoindolin-3-one underwent deamination on reaction with epoxides under mild conditions.Amide group of the substrate reacted slower with epoxide than the dimethylamino grouping whilst the alkanolamide was formed with a great excess of the epoxide only.Of epoxides used in the reaction 1,2-epoxy-3-phenoxypropane, 3-decyloxy-1,2-epoxypropane and 3-chloro-1,2-epoxypropane, the first was found to react most rapidly.