76306-70-2

Basic information

• Product Name: 1,2-BIS(3,4-DIMETHOXYPHENYL)ETHYLFORMAMIDE
• Synonyms: 1,2-BIS(3,4-DIMETHOXYPHENYL)ETHYLFORMAMIDE
• CAS NO: 76306-70-2
• Molecular Formula: C₁₉H₂₃NO₅
• Molecular Weight: 345.39
• Mol File: 76306-70-2.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,2-BIS(3,4-DIMETHOXYPHENYL)ETHYLFORMAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-BIS(3,4-DIMETHOXYPHENYL)ETHYLFORMAMIDE(76306-70-2)
• EPA Substance Registry System: 1,2-BIS(3,4-DIMETHOXYPHENYL)ETHYLFORMAMIDE(76306-70-2)

Safety Data

• Hazardous Substances Data: 76306-70-2(Hazardous Substances Data)

Upstream product

• 4927-55-3 1,2-bis(3,4-dimethoxyphenyl)ethanone 
• 540-69-2 ammonium formate 
• 77287-34-4 formamide 

Downstream Products

• 5471-40-9 3,4,3',4'-tetramethoxy-bibenzyl-α-ylamine 
• 69504-70-7 3-(3,4-dimethoxyphenyl)-6,7-dimethoxyisoquinoline 
• 20232-47-7 3-(3,4-dimethoxyphenyl)-6,7-dimethoxy-3,4-dihydroisoquinoline 
• 18513-98-9 3,4,3',4'-Tetramethoxystilben 
• 76306-53-1 1-(3,4-Dimethoxy-benzyl)-2,3-bis-(3,4-dimethoxy-phenyl)-5,6-dimethoxy-indan 
• 87419-46-3 3-(3,4-Dimethoxy-phenyl)-6,7-dimethoxy-3,4-dihydro-isoquinoline; hydrochloride 
• 90402-70-3 N-<2-(2-bromo-4,5-dimethoxyphenyl)-1-(3,4-dimethoxyphenyl)ethyl>formamide 
• 84573-13-7 (E)-1-(2-bromo-4,5-dimethoxyphenyl)-2-(3,4-dimethoxyphenyl)ethylene 
• 76306-62-2 N-<1,2-bis(3,4-dimethoxyphenyl)ethyl>acetamide 
• 87419-45-2 N-<1,2-bis(3,4-dimethoxyphenyl)ethyl>phenylacetamide 
• 76306-43-9 3,4-dihydro-6,7-dimethoxy-3-(3,4-dimethoxyphenyl)-1-methylisoquinoline 
• 135365-11-6 5-(3,4-Dimethoxy-phenyl)-8,9-dimethoxy-6,10b-dihydro-5H-oxazolo[2,3-a]isoquinoline-2,3-dione 
• 135365-12-7 5-(3,4-Dimethoxy-phenyl)-8,9-dimethoxy-10b-methyl-6,10b-dihydro-5H-oxazolo[2,3-a]isoquinoline-2,3-dione 
• 91486-74-7 3-(3,4-dimethoxyphenyl)-6,7-dimethoxy-3,4-dihydroisoquinoline methiodide 

Relevant articles and documents

Towards the rehabilitation of the Leuckart reductive amination reaction using microwave technology

Leuckart reductive amination of carbonyl compounds was dramatically enhanced with respect to conventional heating by a specific microwave effect when the reaction was performed, under solvent-free conditions, in a monomode microwave reactor. Excellent iso

A Modified Bischler-Napieralski Procedure for the Synthesis of 3-Aryl-3,4-dihydroisoquinolines

A modification of the Bischler-Napieralski reaction for the cyclization of (1,2-diphenylethyl)amides to the 3-aryl-3,4-dihydroisoquinolines is presented.Elimination of the amide group as the nitrile via the retro-Ritter reaction is avoided by its conversion to an N-acyliminium intermediate with oxalyl chloride-FeCl3.Removal of the oxalyl group in refluxing MeOH-sulfuric acid provides the 3,4-dihydroisoquinolines in moderate to high yields.The method is also highly effective with (2-phenylethyl)amides.