79062-23-0

Basic information

• Product Name: 2H-Pyran-2-one, 4-[(2-aminophenyl)amino]-5,6-dihydro-6-methyl-
• CAS NO: 79062-23-0
• Molecular Formula: C12H14N2O2
• Molecular Weight: 218.255
• Mol File: 79062-23-0.mol

Chemical Properties

• CAS DataBase Reference: 2H-Pyran-2-one, 4-[(2-aminophenyl)amino]-5,6-dihydro-6-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 2H-Pyran-2-one, 4-[(2-aminophenyl)amino]-5,6-dihydro-6-methyl-(79062-23-0)
• EPA Substance Registry System: 2H-Pyran-2-one, 4-[(2-aminophenyl)amino]-5,6-dihydro-6-methyl-(79062-23-0)

Safety Data

• Hazardous Substances Data: 79062-23-0(Hazardous Substances Data)

Upstream product

• 33177-29-6 5,6-dihydro-4-hydroxy-6-methyl-2H-pyran-2-one 
• 95-54-5 1,2-diamino-benzene 

Downstream Products

• 131035-20-6 9,10-dihydro-9-methyl-7-oxo<3,4-c>pyrano-6-(parachlorophenyl)-(11H)-5,6-dihydrobenzodiazepine 
• 116761-14-9 3-methyl-11-(2-chlorophenyl)-3,4,10,11-tetrahydro-1H,5H-pyrano<4,3-b><1,5>benzodiazepin-1-one 
• 116761-13-8 3-methyl-11-phenyl-3,4,10,11-tetrahydro-1H,5H-pyrano<4,3-b><1,5>benzodiazepin-1-one 
• 131035-21-7 9,10-dihydro-9-methyl-7-oxo<3,4-c>pyrano-6-(parabromophenyl)-(11H)-5,6-dihydrobenzodiazepine 
• 116761-16-1 3-methyl-11-(3-methylphenyl)-3,4,10,11-tetrahydro-1H,5H-pyrano<4,3-b><1,5>benzodiazepin-1-one 
• 131035-19-3 9,10-dihydro-9-methyl-7-oxo<3,4-c>pyrano-6-(p-methoxyphenyl)-(11H)-5,6-dihydrobenzodiazepine 
• 116761-15-0 3-methyl-11-(4-nitrophenyl)-3,4,10,11-tetrahydro-1H,5H-pyrano<4,3-b><1,5>benzodiazepin-1-one 

Relevant articles and documents

Synthesis of tetracyclic pyrano[4,3-b]-6H-imidazo[1,2-a] [1,5]benzodiazepines

A synthetic route to tetracyclic pyrano[4,3-b]-imidazo[1,2-a][1,5] benzodiazepines is described. The key is the intramolecular cyclization using cyanogen bromide of enaminones, obtained from reaction of pyrone or tetronic acid with o-phenylenediamine deri

Reactivity studies on 4-aminopyrones: Access to benzimidazole and benzimidazolone derivatives

Reaction of pyrone 1a or tetronic acid 1b with o-phenylenediamine derivatives gave enaminone compounds 2. When reacting with different electrophiles, these intermediates allowed versatile access to different heterocyclic structures: when DMA derivatives o

Structure et syntheses nouvelles dans la serie des amino-4-dihydro-5,6- methyl-6 pyrones-2

Primary and secondary amines react with 4-hydroxy-5,6-dihydro-2-pyrones at position 4, and not at position 2 as previously indicated.However, a new series of compounds is obtained by this reaction, some of them exhibiting therapeutic properties.Reactiviti