96237-96-6

Basic information

• Product Name: Benzoic acid, 2,3-dibromo-, 2-(4-nitrobenzoyl)hydrazide
• CAS NO: 96237-96-6
• Molecular Formula: C14H9Br2N3O4
• Molecular Weight: 443.051
• Mol File: 96237-96-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 2,3-dibromo-, 2-(4-nitrobenzoyl)hydrazide(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 2,3-dibromo-, 2-(4-nitrobenzoyl)hydrazide(96237-96-6)
• EPA Substance Registry System: Benzoic acid, 2,3-dibromo-, 2-(4-nitrobenzoyl)hydrazide(96237-96-6)

Safety Data

• Hazardous Substances Data: 96237-96-6(Hazardous Substances Data)

Upstream product

• 96237-90-0 2-bromo-3-methylaniline hydrobromide 
• 61563-25-5 2,3-dibromotoluene 
• 96237-92-2 2,3-dibromobenzoyl chloride 
• 636-97-5 N-amino-(4-nitrophenyl)carboxamide 

Relevant articles and documents

Substitution Reactions of Phenylated Aza-Heterocycles. Part 2. Bromination of Some 2,5-Diaryl-1,3,4-oxadiazoles

Electrophilic bromination of the title compounds may be achieved using either bromine in oleum, or bromine and potassium bromate in a sulphuric-acetic acid mixture.Under the milder reaction conditions provided by the latter, 2-(p-nitrophenyl)-5-phenyl-1,3,4-oxadiazole (2), the model compound used in this study, is mono- and di-brominated in the phenyl ring.In the first bromination step, all three monobromo-isomers are produced in appreciable amount.The orientation of the second bromination is controlled entirely by the first bromine and not by the oxadiazole substituent: this is confirmed by a separate study of the bromination of the three monobromo-compounds (3a-3c).