402737-97-7

Basic information

• Product Name: N-(3,4-dimethoxyphenylethyl)-2-(4-nitrophenoxy)acetamide
• Synonyms: N-(3,4-dimethoxyphenylethyl)-2-(4-nitrophenoxy)acetamide
• CAS NO: 402737-97-7
• Molecular Weight: 360.367
• Mol File: 402737-97-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-(3,4-dimethoxyphenylethyl)-2-(4-nitrophenoxy)acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(3,4-dimethoxyphenylethyl)-2-(4-nitrophenoxy)acetamide(402737-97-7)
• EPA Substance Registry System: N-(3,4-dimethoxyphenylethyl)-2-(4-nitrophenoxy)acetamide(402737-97-7)

Safety Data

• Hazardous Substances Data: 402737-97-7(Hazardous Substances Data)

Upstream product

• 120-20-7 2-(3,4-dimethoxyphenyl)-ethylamine 
• 100-02-7 4-nitro-phenol 
• 14301-31-6 2-chloro-N-(2-(3,4-dimethoxyphenyl)ethyl)acetamide 

Downstream Products

• 887201-39-0 6,7-dimethoxy-1-((4-nitrophenoxy)methyl)-1,2,3,4-tetrahydroisoquinoline 
• 449766-06-7 ((3-bromophenyl)(6,7-dimethoxy-1-((4-nitrophenoxy)-methyl)-3,4-dihydroisoquinolin-2(1H)-yl)methanone) 
• 449765-74-6 (3-chlorophenyl)(6,7-dimethoxy-1-((4-nitrophenoxy)-methyl)-3,4-dihydroisoquinolin-2(1H)-yl)methanone 
• 449765-68-8 (6,7-dimethoxy-1-((4-nitrophenoxy)methyl)-3,4-dihydroisoquinolin-2(1H)-yl)(phenyl)methanone 
• 1443828-43-0 (3-bromophenyl)(6,7-dimethoxy-1-((4-(methylamino)-phenoxy)methyl)-3,4-dihydroisoquinolin-2(1H)-yl)methanone 
• 1443828-42-9 (3-chlorophenyl)(6,7-dimethoxy-1-((4-(methylamino)-phenoxy)methyl)-3,4-dihydroisoquinolin-2(1H)-yl)methanone 
• 1443828-41-8 ((1-((4-aminophenoxy)methyl)-6,7-dimethoxy-3,4-dihydroisoquinolin-2(1H)-yl)(3-bromophenyl)methanone) 
• 1443828-40-7 ((1-((4-aminophenoxy)methyl)-6,7-dimethoxy-3,4-dihydroisoquinolin-2(1H)-yl)(3-chlorophenyl)methanone) 
• 1443828-39-4 ((1-((4-aminophenoxy)methyl)-6,7-dimethoxy-3,4-dihydroisoquinolin-2(1H)-yl)(phenyl)methanone) 
• 1443827-99-3 C₁₈H₁₈N₂O₅ 
• 1443828-73-6 C₁₈H₂₂N₂O₄ 

Relevant articles and documents

Synthesis and structure activity relationship of tetrahydroisoquinoline- based potentiators of GluN2C and GluN2D containing N-Methyl-D-aspartate receptors

We describe here the synthesis and evaluation of a series of tetrahydroisoquinolines that show subunit-selective potentiation of NMDA receptors containing the GluN2C or GluN2D subunits. Bischler-Napieralski conditions were employed in the key step for the