2348-02-9

Basic information

• Product Name: 2-(3-benzyloxyphenyl)-N-(3,4-dimethoxyphenethyl)acetamide
• Synonyms: 2-(3-benzyloxyphenyl)-N-(3,4-dimethoxyphenethyl)acetamide
• CAS NO: 2348-02-9
• Molecular Weight: 405.494
• Mol File: 2348-02-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-(3-benzyloxyphenyl)-N-(3,4-dimethoxyphenethyl)acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(3-benzyloxyphenyl)-N-(3,4-dimethoxyphenethyl)acetamide(2348-02-9)
• EPA Substance Registry System: 2-(3-benzyloxyphenyl)-N-(3,4-dimethoxyphenethyl)acetamide(2348-02-9)

Safety Data

• Hazardous Substances Data: 2348-02-9(Hazardous Substances Data)

Upstream product

• 120-20-7 2-(3,4-dimethoxyphenyl)-ethylamine 
• 59756-83-1 2-(3-(benzyloxy)phenyl)acetyl chloride 
• 100-39-0 benzyl bromide 
• 1860-58-8 3-benzyloxyphenylacetic acid 
• 1700-30-7 (3-(benzyloxy)phenyl)methanol 
• 1700-31-8 3-benzyloxybenzyl bromide 
• 1700-37-4 3-Benzyloxybenzaldehyde 
• 621-37-4 m-hydroxyphenylacetic acid 
• 100-83-4 meta-hydroxybenzaldehyde 
• 100-44-7 benzyl chloride 

Downstream Products

• 109250-11-5 1-(3-hydroxybenzyl)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline 
• 1718-79-2 1-(3-benzyloxybenzyl)-6,7-dimethoxy-2-methyl-1,2,3,4-tetrahydroisoquinoline 
• 1871-07-4 1,2,3,4-tetrahydro-6,7-dimethoxy-1-(3-methoxybenzyl)-2-methylisoquinoline 
• 1718-82-7 rac-1-(3-hydroxybenzyl)-6,7-dimethoxy-2-methyl-1,2,3,4-tetrahydroisoquinoline 
• 142795-15-1 3-(6,7-Dimethoxy-1,2,3,4-tetrahydro-isoquinolin-1-ylmethyl)-phenol; hydrochloride 
• 142741-12-6 1-(3-benzyloxybenzyl)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline 
• 1834-16-8 1-(3-benzyloxy-benzyl)-6,7-dimethoxy-3,4-dihydro-isoquinoline 

Relevant articles and documents

Enantioselective Oxidative Aerobic Dealkylation of N-Ethyl Benzylisoquinolines by Employing the Berberine Bridge Enzyme

N-Dealkylation methods are well described for organic chemistry and the reaction is known in nature and drug metabolism; however, to our knowledge, enantioselective N-dealkylation has not been yet reported. In this study, exclusively the (S)-enantiomers o

(R)-(+)-NORANICANINE A NEW TYPE OF TRIOXYGENATED BENZYLISOQUINOLINE ISOLATION AND SYNTHESIS

(R)-(+)-Noranicanine (1a), a new type of benzylisoquinoline precursor was isolated from Aniba canelilla (Lauraceae) and its structure was determined by means of spectroscopic data as well as by synthesis.