153684-35-6

Basic information

• Product Name: 2-phenyl-4H-naphth<1,2-d><1,3>oxazin-4-one
• Synonyms: 2-phenyl-4H-naphth<1,2-d><1,3>oxazin-4-one
• CAS NO: 153684-35-6
• Molecular Weight: 273.291
• Mol File: 153684-35-6.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2-phenyl-4H-naphth<1,2-d><1,3>oxazin-4-one(CAS DataBase Reference)
• NIST Chemistry Reference: 2-phenyl-4H-naphth<1,2-d><1,3>oxazin-4-one(153684-35-6)
• EPA Substance Registry System: 2-phenyl-4H-naphth<1,2-d><1,3>oxazin-4-one(153684-35-6)

Safety Data

• Hazardous Substances Data: 153684-35-6(Hazardous Substances Data)

Upstream product

• 94208-69-2 Acetophenon-1-naphthyl-hydrazon 
• 98-86-2 acetophenone 
• 2243-55-2 1-(1-naphthyl)hydrazine 
• 33555-17-8 2-phenyl-1H-benzo[g]indole 
• 1431098-45-1 C₁₈H₁₂BrNO₂ 
• 86-57-7 1-Nitronaphthalene 
• 3100-67-2 1-amino-2-naphthalenecarbonitrile 
• 4919-43-1 1-amino-2-naphthoic acid 
• 98-88-4 benzoyl chloride 

Downstream Products

• 154848-99-4 1--2-(2'-fluorobenzoyl)naphthalene 
• 154849-00-0 5-(2-fluorophenyl)-1,3-dihydronaphtho<1,2-e><1,4>diazepin-2-one 
• 153684-36-7 1-amino-2-(2'-fluorobenzoyl)naphthalene 
• 153684-39-0 1-(N-benzoylamino)-2-(2'-fluorobenzoyl)naphthalene 

Relevant articles and documents

Copper-mediated oxidative tandem reactions with molecular oxygen: Synthesis of 2-arylbenzoxazinone derivatives from indoles

We developed an efficient method for the transformation of indoles by utilizing a copper catalyst and molecular oxygen as the oxidant. The transformation involves a tandem oxidative process of 2-arylindoles. Our reaction afforded a variety of N-benzoyl an

Copper-catalyzed C-N bond formation/rearrangement sequence: Synthesis of 4H-3,1-benzoxazin-4-ones

A facile and efficient copper-catalyzed method for the synthesis of 4H-3,1-benzoxazin-4-one derivatives has been developed. This procedure is based on a tandem intramolecular C-N coupling/rearrangement process. This method would provide a new and useful strategy for construction of N-heterocycles.

The Regiospecific Synthesis Of Ortho Aminonaphthophenones Via The Addition Of Carbanions To Naphthoxazin-4-Ones

The conversion of nitronaphthalenes (see 4a and 4b) into the corresponding ortho aminonaphthylnitriles (5a and 5b) via the process of Tomioka, when combined with the addition of carbanions to the intermediate naphthoxazin-4-ones, provided a route to ortho aminonaphthophenones (7a) and (7b).These key intermediates were employed to synthesize the benzfused 2'-fluoro-1,4-benzodiazepines (1-3).