1924-19-2

Basic information

• Product Name: 5H-Benzo[a]phenoxazin-5-one
• CAS NO: 1924-19-2
• Molecular Formula: C16H9NO2
• Molecular Weight: 247.253
• Mol File: 1924-19-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 5H-Benzo[a]phenoxazin-5-one(CAS DataBase Reference)
• NIST Chemistry Reference: 5H-Benzo[a]phenoxazin-5-one(1924-19-2)
• EPA Substance Registry System: 5H-Benzo[a]phenoxazin-5-one(1924-19-2)

Safety Data

• Hazardous Substances Data: 1924-19-2(Hazardous Substances Data)

Upstream product

• 64-17-5 ethanol 
• 27828-56-4 4-(phenylamino)naphthalene-1,2-dione 
• 83-72-7 2-hydroxynaphtho-1,4-quinone 
• 95-55-6 2-amino-phenol 
• 117-80-6 2,3-Dichloro-1,4-naphthoquinone 
• 90-30-2 N-phenyl-1-naphthylamine 
• 110-86-1 pyridine 
• 51-19-4 2-aminophenol hydrochloride 

Downstream Products

• 39676-57-8 9-phenylsulfanyl-benzo[a]phenoxazin-5-one 
• 39676-56-7 9-p-tolylsulfanyl-benzo[a]phenoxazin-5-one 
• 39676-58-9 9-(4-nitro-phenylsulfanyl)-benzo[a]phenoxazin-5-one 
• 89984-89-4 6-cyclohexyl-5H-benzophenoxazin-5-one 
• 78490-02-5 6-Phenylsulfanyl-benzo[a]phenoxazin-5-one 
• 96103-64-9 6-(2-Methyl-benzyl)-benzo[a]phenoxazin-5-one 

Relevant articles and documents

Synthesis, spectral characterization, crystal structure, cytotoxicity and apoptosis—Inducing activity of two derivatives of 2-hydroxy-1,4-naphthaquinone

A phenaxazone compound [5H-Benzo[a]phenoxazin-5-one (BP)] along with an aminoquinone[2-[(o-hydroxyphenyl)amino]-1,4-naphthaquinone (HAN)] derivatives were synthesized from lawsone using ultrasound irradiation technique. The structure of the compounds were

Reactivity and Structure of N-Phenyl-1-naphthylamines and Related Compounds. Part 3. Reaction with Oxygen-centred Radicals

Comparison is made between products obtained by oxidation of N-phenyl-1-naphthylamines and 1-naphthyl phenyl nitroxides with peroxyl radicals.It is concluded that oxidation of the amines does not proceed to a considerable extent via the nitroxides.Comparison is also made of products obtained from these amines and nitroxides by oxidation with Fremy's salt.