5100-23-2

Upstream product

• 118-48-9 isatoic anhydride 
• 118-92-3 anthranilic acid 
• 503-38-8 trichloromethyl chloroformate 

Downstream Products

• 58418-25-0 2-tert-Butylimino-1,2-dihydro-4H-3,1-benzoxazin-4-on 
• 5100-29-8 N-Methyl-2-isocyanato-benzanilid 
• 71526-47-1 4,4-diphenyl-1,4-dihydro-3,1-benzoxazin-2(1H)-one 
• 6268-38-8 N-methoxycarbonyl-anthranilic acid 
• 1701-95-7 3-(2-Carboxyphenyl)-1,2,3,4-tetrahydroquinazoline-2,4-dione 
• 51364-45-5 dimethyl 2,2'-bisbenzoate 
• 719-59-5 5-chloro-2-aminobenzophenone 
• 117192-53-7 3-Methoxy-5-(2-carbomethoxyphenyl)-4H,6H-3,1,5-benzoxadiazocine-4,6-dione 
• 4471-39-0 N,N'-Di(2-carboxyphenyl)urea 
• 13969-02-3 5H,12H-Quinazolino<3,2-a><3,1>benzoxazine-5,12-dione 
• 118-48-9 isatoic anhydride 
• 117192-52-6 2-[(Z)-2-Benzoyl-4-chloro-phenylimino]-1,2-dihydro-benzo[d][1,3]oxazin-4-one 
• 106537-13-7 2-chloro-6,12-diphenyl-dibenzo<1,5>diazocine 
• 106537-09-1 (2-{[1-(2-Amino-phenyl)-1-phenyl-meth-(Z)-ylidene]-amino}-5-chloro-phenyl)-phenyl-methanone 

Relevant academic research and scientific papers

Synthese de tertiobutylcetones α-azotees de type =N-C(R1)(R2)-CO-C(CH3)3

The α-nitrogen-ketones 2, 3 and 4 were prepared from α-bromoketones.These were synthesized by the bromination of the ketones which had been obtained by the pinacolone or benzyltertiobutylketone alkylation from the corresponding halo-derivatives.We have observed that the bromination of the ketones depends to some extent upon the nature of these compounds.