86672-55-1

Basic information

• Product Name: 2-((4-methoxyphenyl)amino)-4H-benzo[d][1,3]oxazin-4-one
• Synonyms: 2-((4-methoxyphenyl)amino)-4H-benzo[d][1,3]oxazin-4-one
• CAS NO: 86672-55-1
• Molecular Weight: 268.272
• Mol File: 86672-55-1.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 2-((4-methoxyphenyl)amino)-4H-benzo[d][1,3]oxazin-4-one(CAS DataBase Reference)
• NIST Chemistry Reference: 2-((4-methoxyphenyl)amino)-4H-benzo[d][1,3]oxazin-4-one(86672-55-1)
• EPA Substance Registry System: 2-((4-methoxyphenyl)amino)-4H-benzo[d][1,3]oxazin-4-one(86672-55-1)

Safety Data

• Hazardous Substances Data: 86672-55-1(Hazardous Substances Data)

Upstream product

• 34956-06-4 methyl N-(4-methoxyphenyl)dithiocarbamate 
• 37960-65-9 potassium anthranilate 
• 201230-82-2 carbon monoxide 
• 54467-95-7 1-azido-2-iodo-benzene 
• 104-94-9 4-methoxy-aniline 
• 14223-47-3 4-methoxyphenyl isoselenocyanate 
• 118-92-3 anthranilic acid 
• 179039-70-4 ethyl 2-(triphenylphosphoranylidene-amino)benzoate 
• 5416-93-3 4-Methoxyphenyl isocyanate 

Relevant articles and documents

Pd/C-Catalyzed Carbonylative Synthesis of 2-Aminobenzoxazinones from 2-Iodoaryl Azides and Amines

A palladium-catalyzed carbonylative procedure for the synthesis of 2-aminobenzoxazinones from 1-azido-2-iodobenzenes and amines has been developed. A broad range of 2-aminobenzoxazinone derivatives were prepared in moderate to excellent yields by using Pd

2-amino-benzoxazinone derivatives for the treatment of obesity

The use of a compound comprising formula (I): (I) or a salt, ester, amide or prodrug therof in the inhibition of an enzyme whose preferred mode of action is to catalyse the hydrolysis of an ester functionality, e.g. in the control and inhibition of unwant

Tetrabutylammonium fluoride promoted intramolecular nucleophilic attack of an ester group on a carbodiimide: Preparation of 1,3-oxazolin-5-ones and 3,1-benzoxazin-4-ones

Functionalized carbodiimides bearing an ester group either at the α or β position undergo cyclization in the presence of tetrabutylammonium fluoride (TBAF) under mild conditions to give 1,3-oxazolin-5-ones or 3,1-benzoxazin-4-ones in synthetically useful yields.