92197-18-7

Basic information

• Product Name: N, N-diisopropyl-O-benzoyl hydroxylamine
• Synonyms: N, N-diisopropyl-O-benzoyl hydroxylamine
• CAS NO: 92197-18-7
• Molecular Weight: 221.299
• Mol File: 92197-18-7.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: N, N-diisopropyl-O-benzoyl hydroxylamine(CAS DataBase Reference)
• NIST Chemistry Reference: N, N-diisopropyl-O-benzoyl hydroxylamine(92197-18-7)
• EPA Substance Registry System: N, N-diisopropyl-O-benzoyl hydroxylamine(92197-18-7)

Safety Data

• Hazardous Substances Data: 92197-18-7(Hazardous Substances Data)

Upstream product

• 108-18-9 diisopropylamine 
• 94-36-0 dibenzoyl peroxide 

Downstream Products

• 4107-98-6 N,N-diisopropylaniline 
• 5440-69-7 N-isopropylbenzamide 
• 79606-44-3 4-fluoro-N,N-diisopropylbenzamide 
• 6937-52-6 N,N-diisopropyl-4-methylbenzamide 
• 1684-07-7 3,4-diphenyl-isochromen-1-one 
• 13330-86-4 4-bromo-N,N-bis(propan-2-yl)aniline 
• 29275-99-8 4-nitro-N,N-bis(propan-2-yl)aniline 
• 6863-97-4 N,N-diisopropyl(2-methylphenyl)amine 
• 124935-88-2 N,N-diisopropyl-3-(2-methoxy-5-methylphenyl)-3-phenylpropan-1-amine 
• 1372405-11-2 N,N-diisopropyl-4-phenylbutan-1-amine 
• 1372404-94-8 4-(4-bromophenyl)-N,N-diisopropylbutan-1-amine 
• 1372404-93-7 N,N-diisopropyl-4-(4-methoxylphenyl)butan-1-amine 
• 132514-79-5 N,N-Diisopropyl-4-methoxyaniline 
• 153688-91-6 4-iodo-N,N-diisopropylaniline 

Relevant articles and documents

Palladium/norbornene-mediated tandem C-H amination/C-I alkenylation reaction of aryl iodides with secondary cyclic O-benzoyl hydroxylamines and activated terminal olefins

A novel palladium-catalyzed norbornene-mediated three-component reaction for the construction of ortho-alkenyl aromatic tertiary amines has been achieved, which represents a useful extension of the Catellani-type tandem ortho-selective C-H amination trans

Copper-Catalyzed Three-Component Carboamination of Arynes: Expeditious Synthesis of o-Alkynyl Anilines and o-Benzoxazolyl Anilines

A copper-catalyzed three-component reaction of in situ formed arynes, terminal alkynes, and O-benzoylhydroxylamines has been developed. By adjusting reaction conditions, the nucleophiles in this transformation can be extended from terminal alkynes to benzoxazoles. These procedures provide a modular and facile approach to o-alkynyl anilines and o-benzoxazolyl anilines from easily available substrates in only one step.

Synthesis of hindered anilines: Copper-catalyzed electrophilic amination of aryl boronic esters

No longer a hindrance: Copper-catalyzed electrophilic amination of aryl boronic esters is accomplished under mild reaction conditions using 2.5-5.0 mol % of a catalyst derived from copper tert-butoxide and Xantphos ligand (see scheme). The reaction tolerates a wide range of functional groups and can be used to prepare some of the most hindered anilines made to date. Copyright