39964-84-6

Basic information

• Product Name: Ethanamine, 2,2-dimethoxy-N-[(3-methoxyphenyl)methylene]-
• Synonyms: (3-Methoxy-benzylidenamino)-acetaldehyd-dimethylacetal;Ethanamine,2,2-dimethoxy-N-[(3-methoxyphenyl)methylene]
• CAS NO: 39964-84-6
• Molecular Formula: C12H17NO3
• Molecular Weight: 223.26800
• Mol File: 39964-84-6.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Ethanamine, 2,2-dimethoxy-N-[(3-methoxyphenyl)methylene]-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanamine, 2,2-dimethoxy-N-[(3-methoxyphenyl)methylene]-(39964-84-6)
• EPA Substance Registry System: Ethanamine, 2,2-dimethoxy-N-[(3-methoxyphenyl)methylene]-(39964-84-6)

Safety Data

• Hazardous Substances Data: 39964-84-6(Hazardous Substances Data)

Upstream product

• 591-31-1 3-methoxy-benzaldehyde 
• 22483-09-6 2,2-dimethoxyethylamine 

Downstream Products

• 95333-54-3 1-(3-Methoxy-benzyl)-1,3-dihydro-imidazole-2-thione 
• 95333-50-9 1-(3-Hydroxy-benzyl)-1,3-dihydro-imidazole-2-thione 
• 73894-30-1 (2,2-Dimethoxy-ethyl)-[1-(3-methoxy-phenyl)-2-thiophen-2-yl-ethyl]-methyl-amine 
• 73909-49-6 (2,2-Dimethoxy-ethyl)-[1-(3-methoxy-phenyl)-2-thiophen-3-yl-ethyl]-methyl-amine 
• 103030-70-2 5-methoxy-1,2,3,4-tetrahydro-isoquinoline 
• 43207-78-9 7-methoxy-1,2,3,4-tetrahydroisoquinoline 
• 39989-39-4 7-methoxyisoquinoline 
• 53366-27-1 N-(3-methoxybenzyl)aminoacetaldehyde dimethyl acetal 
• 1344688-57-8 C₁₉H₁₅NO₅ 
• 1344689-11-7 C₁₉H₁₅NO₄ 
• 1344689-08-2 C₁₉H₁₇NO₃ 
• 1344689-06-0 C₂₂H₂₃NO₅ 
• 1344689-04-8 C₂₁H₂₃NO₄ 
• 1344689-01-5 C₂₃H₃₁NO₆ 

Relevant articles and documents

Discovery of 1-arylcarbonyl-6,7-dimethoxyisoquinoline derivatives as glutamine fructose-6-phosphate amidotransferase (GFAT) inhibitors

Through high throughput screening and subsequent hit identification and optimization, we synthesized a series of 1-arylcarbonyl-6,7- dimethoxyisoquinoline derivatives as the first reported potent and reversible GFAT inhibitors. SAR studies of this class o

Improved procedures for large preperation of 6- and 7-oxy-substituted isoquinolines and a convenient work-up protocol for titanium supported reactions

Improved procedures for large scale preparation of oxy-substituted isoquinolines are reported. Moreover, a simple and convenient protocol for alkaline work-up of titanium containing reaction mixtures is given, which is expected to be of general interest even for reactions on a technical scale.

Regioselectivity in the Synthesis of Isoquinolines with Methoxy Activating Groups

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