913985-90-7

Basic information

• Product Name: N-[2-(4-hydroxy-2,3-dimethoxy-phenyl)-ethyl]-acetamide
• Synonyms: N-[2-(4-hydroxy-2,3-dimethoxy-phenyl)-ethyl]-acetamide
• CAS NO: 913985-90-7
• Molecular Weight: 239.271
• Mol File: 913985-90-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-[2-(4-hydroxy-2,3-dimethoxy-phenyl)-ethyl]-acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-[2-(4-hydroxy-2,3-dimethoxy-phenyl)-ethyl]-acetamide(913985-90-7)
• EPA Substance Registry System: N-[2-(4-hydroxy-2,3-dimethoxy-phenyl)-ethyl]-acetamide(913985-90-7)

Safety Data

• Hazardous Substances Data: 913985-90-7(Hazardous Substances Data)

Upstream product

• 52800-47-2 3-(benzyloxy)benzene-1,2-diol 
• 69471-04-1 4-benzyloxy-2,3-dimethoxybenzaldehyde 
• 770686-91-4 4-benzyloxy-2,3-dimethoxyphenethylamine 
• 913985-88-3 4-bromo-2,3-dimethoxy-1-benzyloxybenzene 
• 913985-89-4 N-[2-(4-benzyloxy-2,3-dimethoxy-phenyl)-ethyl]-acetamide 

Downstream Products

• 913985-93-0 (7-allyloxy-5,6-dimethoxy-1-methylene-3,4-dihydro-1H-isoquinolin-2-yl)-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-methanone 
• 913985-91-8 N-[2-(4-allyloxy-2,3-dimethoxy-phenyl)-ethyl]-acetamide 

Relevant articles and documents

The first total synthesis of (±)-annosqualine by means of oxidative enamide-phenol coupling: pronounced effect of phenoxide formation on the phenol oxidation mechanism

The first total synthesis of a spiro-isoquinoline alkaloid, (±)-annosqualine, was established by employing an enamide-phenol coupling of a 1-methylene-1,2,3,4-tetrahydroisoquinoline derivative with a hypervalent iodine reagent, where the formation of the