16095-32-2

Basic information

• Product Name: 1-phenyl-1,2-dihydro-4H-benzo[d][1,3]oxazin-4-one
• Synonyms: 1-phenyl-1,2-dihydro-4H-benzo[d][1,3]oxazin-4-one
• CAS NO: 16095-32-2
• Molecular Weight: 225.247
• Mol File: 16095-32-2.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 1-phenyl-1,2-dihydro-4H-benzo[d][1,3]oxazin-4-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-phenyl-1,2-dihydro-4H-benzo[d][1,3]oxazin-4-one(16095-32-2)
• EPA Substance Registry System: 1-phenyl-1,2-dihydro-4H-benzo[d][1,3]oxazin-4-one(16095-32-2)

Safety Data

• Hazardous Substances Data: 16095-32-2(Hazardous Substances Data)

Upstream product

• 73323-82-7 2-(N-Methyl-N-phenylamino)-benzoic acid 
• 169170-03-0 N-methyl-N-phenylanthranilic acid methyl ester 
• 121-69-7 N,N-dimethyl-aniline 
• 50-00-0 formaldehyd 
• 91-40-7 2-(phenylamino)benzoic acid 

Downstream Products

• 77778-87-1 N-cyanomethyl-N-phenyl-anthranilic acid 
• 16075-09-5 1-phenyl-1,2-dihydro-benzo[d][1,3]thiazin-4-one 
• 131540-79-9 1-phenyl-3-piperazino-1H-indole 
• 85793-69-7 2-<(2-methoxy-2-oxoethyl)phenylamino>benzoic acid methyl ester 
• 85793-68-6 2-<(carboxymethyl)phenylamino>benzoic acid 
• 71711-33-6 3-hydroxy-1-phenyl-1H-indole-2-carboxylic acid methyl ester 
• 16095-54-8 1-phenyl-1,2-dihydro-benzo[d][1,3]thiazine-4-thione 
• 31182-48-6 meso-1,1''-diphenyl-1,2,1'',2''-tetrahydro-dispiro[benzo[d][1,3]thiazine-4,4'-[1,3]dithiolane-5',4''-benzo[d][1,3]thiazine] 

Relevant articles and documents

Pd-Catalyzed Intramolecular Chemoselective C(sp2)-H and C(sp3)-H Activation of N-Alkyl- N-arylanthranilic Acids

A controllable palladium-catalyzed intramolecular C-H activation of N-alkyl-N-arylanthranilic acids has been developed. The methodology allows selective synthesis of 1,2-dihydro-(4H)-3,1-benzoxazin-4-ones and carbazoles from the same starting materials and palladium catalyst. The selectivity is controlled by the oxidant. Silver oxide promotes C(sp3)-H activation/C-O cyclization to provide 1,2-dihydro-(4H)-3,1-benzoxazin-4-ones, while copper acetate contributes to C(sp2)-H activation/decarboxylative arylation to afford carbazoles. This protocol is demonstrated by its wide substrate scope and good functional group tolerance.

Organocatalytic enantioselective amination of 2-substituted indolin-3-ones: A strategy for the synthesis of chiral α-hydrazino esters

An efficient enantioselective α-amination of 2-substituted 3-indolinones has been achieved for the first time using hydroquinidine as a chiral catalyst through an aza-Michael reaction. The desired α-hydrazino esters are obtained in excellent yields with h

Structure-activity relationships of a series of novel (piperazinylbutyl)thiazolidinone antipsychotic agents related to 3-[4-[4-(6- fluorobenzo[b]thien-3-yl)-1-piperazinyl]butyl]-2,5,5-trimethyl-4- thiazolidinone maleate

HP-236 (3-[4-[4-(6-Fluorobenzo[b]thien-3-yl)-1-piperazinyl]butyl]- 2,5,5-trimethyl-4-thiazolidinone maleate; P-9236) (54) displayed a pharmacological profile indicative of potential atypical antipsychotic activity. A series of piperazinyl butyl thiazolidi