40292-19-1

Basic information

• Product Name: Methanone, (4-aminophenyl)(4-bromophenyl)-
• CAS NO: 40292-19-1
• Molecular Formula: C13H10BrNO
• Molecular Weight: 276.132
• Mol File: 40292-19-1.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Methanone, (4-aminophenyl)(4-bromophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Methanone, (4-aminophenyl)(4-bromophenyl)-(40292-19-1)
• EPA Substance Registry System: Methanone, (4-aminophenyl)(4-bromophenyl)-(40292-19-1)

Safety Data

• Hazardous Substances Data: 40292-19-1(Hazardous Substances Data)

Upstream product

• 586-75-4 4-chlorobenzoyl chloride 
• 540-37-4 p-aminoiodobenzene 
• 873-75-6 4-bromobenzenemethanol 
• 62-53-3 aniline 
• 122-04-3 4-nitro-benzoyl chloride 
• 100-14-1 4-nitrobenzyl chloride 
• 108-86-1 bromobenzene 
• 40292-15-7 4-bromophenyl(4-nitrophenyl)methanone 

Downstream Products

• 1321599-99-8 4-bromo-4'-aminobenzophenone hydrazone 
• 139442-23-2 N-[4-(4-bromobenzoyl)phenyl]-5-ethylisoxazole-4-carboxamide 
• 25782-57-4 (4-aminophenyl)(phenyl)methanol 
• 71961-48-3 C₂₆H₂₀Br₂N₄ 
• 71968-74-6 C₂₇H₂₂BrClN₄ 
• 71968-75-7 C₂₈H₂₅BrN₄ 
• 71968-91-7 C₂₉H₂₇BrN₄ 
• 71968-76-8 C₂₆H₁₉BrCl₂N₄ 
• 71968-65-5 C₂₇H₂₃BrN₄O 
• 71968-63-3 C₂₇H₂₃BrN₄ 
• 71968-62-2 C₂₆H₂₀BrClN₄ 
• 4369-50-0 4-hydroxyphenyl-(4-bromo-phenyl)-methanone 
• 351003-30-0 4-ethoxy-4'-bromo-benzophenone 

Relevant articles and documents

Synthesis of Benzophenone Nucleosides and Their Photocatalytic Evaluation for [2+2] Cycloaddition in Aqueous Media

Four benzophenone nucleosides that are para-substituted (-NH2, -NMe2, -OMe, and -Me) in relation to the carbonyl group were synthesized and characterized by their optical properties. The electron-donating character of the substituent

Coumarin-surfactant modified polyoxometalate catalyzed cross dehydrogenative coupling of benzyl alcohol with the: Para -C-H of unprotected aniline

This paper presents a novel method for synthesizing para-aminobenzophenone and its derivatives (p-ABPs) using a coumarin-surfactant modified polyoxometalate as the catalyst. Preliminary mechanistic studies indicate that the reaction has undergone an oxidative cross dehydrogenative coupling process. This method has the advantages of an easy process, a convenient raw material source, safe and green oxidants, and tolerances of several functional groups.

Studies on the Insecticidal Activities of Some New N-Benzoyl-N'-Arylureas

This paper reports the synthesis and the insecticidal activities of some N-benzoyl-N'-arylureas 4-arylsubstituted with alkylated or halogenated aroyl moieties. The compounds, tested against some representative insect species, displayed very high activity against Aedes aegypti, especially the halosubstituted derivatives. None of the newly synthesized compounds showed genotoxic activity in the Bacillus subtilis rec-assay and in the Salmonella-microsome test.