796074-04-9

Basic information

• Product Name: (2,3-dimethoxy-phenyl)-acetic acid-(2,3-dimethoxy-phenethylamide)
• Synonyms: (2,3-dimethoxy-phenyl)-acetic acid-(2,3-dimethoxy-phenethylamide)
• CAS NO: 796074-04-9
• Molecular Weight: 359.422
• Mol File: 796074-04-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2,3-dimethoxy-phenyl)-acetic acid-(2,3-dimethoxy-phenethylamide)(CAS DataBase Reference)
• NIST Chemistry Reference: (2,3-dimethoxy-phenyl)-acetic acid-(2,3-dimethoxy-phenethylamide)(796074-04-9)
• EPA Substance Registry System: (2,3-dimethoxy-phenyl)-acetic acid-(2,3-dimethoxy-phenethylamide)(796074-04-9)

Safety Data

• Hazardous Substances Data: 796074-04-9(Hazardous Substances Data)

Upstream product

• 3213-29-4 2,3-dimethoxyphenethylamine 
• 6831-56-7 2',3'-dimethoxyphenylacetyl chloride 
• 3893-01-4 2,3-dimethoxybenzyl chloride 
• 110600-36-7 (2,3-dimethoxy-phenyl)-acetaldehyde-oxime 
• 2815-67-0 2,3-dimethoxynitrostyrene 
• 4468-57-9 2-(2,3-dimethoxyphenyl)acetonitrile 
• 90-53-9 2,3-dimethoxyphenylacetic acid 

Downstream Products

• 872788-11-9 1-(2,3-dimethoxy-benzyl)-5,6-dimethoxy-3,4-dihydro-isoquinoline 
• 6957-27-3 3,4-dihydropapaverine 

Relevant articles and documents

Selective inhibition of calcium entry induced by benzylisoquinolines in rat smooth muscle

The mechanism of relaxant activity of six benzylisoquinolines was examined in order to determine the minimal structural requirements that enable these compounds to have either a non-specific action like papaverine or an inhibitory activity on calcium entry via potential-operated channels. All the alkaloids tested totally or partially relaxed KCl-depolarized rat uterus and inhibited oxytocin-induced rhythmic contractions. Only glaucine and laudanosine inhibited K+-induced uterine contractions more than oxytocin-induced uterine contractions. In Ca+-free medium, sustained contractions induced by oxytocin or vanadate were relaxed by the alkaloids tested except for glaucine and laudanosine indicating no inhibitory effect on intracellular calcium release. Those alkaloids containing an unsaturated heterocyclic ring (papaverine, papaverinol, papaveraldine, N-methylpapaverine and dehydropapaverine) exhibited a more specific activity than those with a tetrahydroisoquinoline ring.