212512-28-2

Basic information

• Product Name: 3,5-dimethoxy-2-(methoxyacetyl)aniline
• Synonyms: 3,5-dimethoxy-2-(methoxyacetyl)aniline
• CAS NO: 212512-28-2
• Molecular Weight: 225.244
• Mol File: 212512-28-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3,5-dimethoxy-2-(methoxyacetyl)aniline(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-dimethoxy-2-(methoxyacetyl)aniline(212512-28-2)
• EPA Substance Registry System: 3,5-dimethoxy-2-(methoxyacetyl)aniline(212512-28-2)

Safety Data

• Hazardous Substances Data: 212512-28-2(Hazardous Substances Data)

Upstream product

• 1738-36-9 2-methoxyacetonitrile 
• 10272-07-8 3.5-dimethoxyaniline 

Downstream Products

• 1027049-64-4 4-butyl-N-(3,5-dimethoxy-2-methoxyacetyl-phenyl)-benzamide 
• 1025809-47-5 N-(3,5-dimethoxy-2-methoxyacetyl-phenyl)-3,4,5-trimethoxy-benzamide 
• 1026360-58-6 N-(3,5-dimethoxy-2-methoxyacetyl-phenyl)-3,4-difluoro-benzamide 
• 1026001-25-1 N-(3,5-dimethoxy-2-methoxyacetyl-phenyl)-3,5-difluoro-benzamide 
• 305834-42-8 N-(3,5-dimethoxy-2-methoxyacetyl-phenyl)-benzamide 
• 1027894-21-8 N-(3,5-dimethoxy-2-methoxyacetyl-phenyl)-4-methyl-benzamide 
• 305834-44-0 N-(3,5-dimethoxy-2-methoxyacetyl-phenyl)-4-methoxy-benzamide 
• 1027033-40-4 4-amino-N-(3,5-dimethoxy-2-methoxyacetyl-phenyl)-benzamide 
• 1025980-36-2 4-tert-butyl-N-(3,5-dimethoxy-2-methoxyacetyl-phenyl)-benzamide 
• 1026457-04-4 N-(3,5-dimethoxy-2-(2-methoxyacetyl)phenyl)-3,4-dimethoxybenzamide 
• 1025913-65-8 2-(4-amino-phenyl)-3,5,7-trimethoxy-1H-quinolin-4-one 
• 1026632-68-7 2-(3,4-difluoro-phenyl)-3,5,7-trimethoxy-1H-quinolin-4-one 
• 1027834-49-6 2-(4-tert-butyl-phenyl)-3,5,7-trimethoxy-1H-quinolin-4-one 
• 1026861-79-9 2-(3,5-dichloro-phenyl)-3,5,7-trimethoxy-1H-quinolin-4-one 

Relevant articles and documents

Synthesis and topoisomerase inhibitory activities of novel aza-analogues of flavones

A series of aza-flavones (3-hydroxy-2-phenyl-4-quinolones) were designed and synthesized as inhibitors of bacterial DNA-gyrase and mammalian topoisomerase II. Structure activity relationships of the compounds against each of the enzymes are discussed.