149220-84-8

Basic information

• Product Name: 2-(2-benzyloxyphenylamino)-3,4,6-trimethoxy-N,N-dimethylbenzamide
• Synonyms: 2-(2-benzyloxyphenylamino)-3,4,6-trimethoxy-N,N-dimethylbenzamide
• CAS NO: 149220-84-8
• Molecular Weight: 436.508
• Mol File: 149220-84-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-(2-benzyloxyphenylamino)-3,4,6-trimethoxy-N,N-dimethylbenzamide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-benzyloxyphenylamino)-3,4,6-trimethoxy-N,N-dimethylbenzamide(149220-84-8)
• EPA Substance Registry System: 2-(2-benzyloxyphenylamino)-3,4,6-trimethoxy-N,N-dimethylbenzamide(149220-84-8)

Safety Data

• Hazardous Substances Data: 149220-84-8(Hazardous Substances Data)

Upstream product

• 149220-82-6 2-iodo-3,4,6-trimethoxy-N,N-dimethylbenzamide 
• 149220-81-5 2,4,5-trimethoxy-N,N-dimethylbenzamide 
• 100-44-7 benzyl chloride 
• 149220-83-7 2-(2-hydroxyphenylamino)-3,4,6-trimethoxy-N,N-dimethylbenzamide 
• 490-64-2 asaronic acid 

Downstream Products

• 149220-86-0 5-benzyloxy-1-hydroxy-3,4-dimethoxy-10-methyl-9(10H)-acridone 
• 86680-32-2 Citrusinine-I 
• 130897-43-7 5-benzyloxy-1,3,4-trimethoxy-10-methyl-9(10H)-acridone 
• 130897-44-8 5-benzyloxy-1-hydroxy-3,4-dimethoxy-9(10H)-acridone 
• 130897-42-6 5-benzyloxy-1,3,4-trimethoxy-9(10H)-acridone 

Relevant articles and documents

Syntheses of the acridone alkaloid citrusinine-I and its derivatives

Citrusinine-I (1), a naturally occurring acridone alkaloid with potent antiviral activity, was synthesized for the first time, via a route involving Ullmann reaction, cyclization, and selective demethylation at the 1-position with boron trifluoride etherate and lithium bromide. 1,5,6-Trihydroxy-3-methoxy-9(10H)-acridone (2a) and 1,5,6-trihydroxy-3-methoxy-10-methyl-9(10H)-acridone (2b) were also synthesized.