32142-34-0

Basic information

• Product Name: 1-phenyl-2-(phenylamino)propane-1-one
• Synonyms: 1-phenyl-2-(phenylamino)propane-1-one
• CAS NO: 32142-34-0
• Molecular Weight: 225.29
• Mol File: 32142-34-0.mol
• Article Data: 15

Chemical Properties

• CAS DataBase Reference: 1-phenyl-2-(phenylamino)propane-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-phenyl-2-(phenylamino)propane-1-one(32142-34-0)
• EPA Substance Registry System: 1-phenyl-2-(phenylamino)propane-1-one(32142-34-0)

Safety Data

• Hazardous Substances Data: 32142-34-0(Hazardous Substances Data)

Upstream product

• 2114-00-3 2-bromo-1-phenyl-1-propanone 
• 62-53-3 aniline 
• 579-07-7 1-Phenylpropane-1,2-dione 
• 32142-35-1 (1-methyl-2-oxo-2-phenyl-ethyl)-phenyl-carbamic acid ethyl ester 
• 4187-87-5 1-Phenyl-2-propyn-1-ol 
• 673-32-5 1-Phenylprop-1-yne 
• 67-56-1 methanol 
• 5883-81-8 2-anilinoacetophenone 
• 70-11-1 α-bromoacetophenone 
• 74-88-4 methyl iodide 
• 64-17-5 ethanol 
• 14088-57-4 2-diazo-1-phenyl-1-propanone 
• 593-95-3 carbonyl dibromide 
• 51388-20-6 4-benzyloxyaniline hydrochloride 

Downstream Products

• 106989-73-5 1-phenyl-1-(phenylamino)propan-2-one 
• 91025-67-1 2-methyl-1,3,5-triphenyl-1H-pyrrole 
• 1022-86-2 2-benzoylindole 
• 1403656-52-9 1,4-diphenyl-3-(3-chlorophenyl)-4-methyl-2-tosylaminopyrrole 
• 1403656-42-7 (E)-2-(3-chlorophenyl)-N-(1-oxo-1-phenylpropan-2-yl)-N-phenyl-N'-tosylacetamidine 
• 29200-10-0 4-methyl-3,5-diphenyl-3H-oxazol-2-one 
• 26309-40-0 2,6-dimethyl-5-phenyl-4H-thieno[3,2-b]pyrrole-3-carboxylic acid ethyl ester 
• 10257-92-8 2-phenyl-3-methyl-1H-indole 
• 74554-45-3 N-(1-methyl-2-oxo-2-phenyl-ethyl)-benzanilide 
• 26381-78-2 2,6-dimethyl-5-phenyl-4H-thieno[3,2-b]pyrrole-3-carboxylic acid 
• 155699-85-7 (1-Methyl-2-oxo-2-phenyl-ethyl)-phenyl-thiocarbamic acid O-phenyl ester 
• 99334-89-1 1-phenyl-2-(phenylimino)propan-1-one 

Relevant articles and documents

Palladium-catalyzed tandem oxidative annulation of α-amino ketones leading to 2-aroylindoles

A simple synthesis of 2-aroylindoles via palladium-catalyzed tandem oxidative annulation directly from α-amino ketones has been developed. In this transformation, two-step reaction including oxidation of α-amino aetones to generate imine intermediates and

Synthesis of α-heterosubstituted ketones through sulfur mediated difunctionalization of internal alkynes

Synthesis of α-heterosubstituted ketones was achieved through sulfur mediated difunctionalization of internal alkynes in one pot. The reaction design involves: phenyl substituted internal alkyne attacking triflic anhydride activated diphenyl sulfoxide to

Highly diastereoselective synthesis of tertiary alcohols via intramolecular Baylis-Hillman reaction using less reactive acrylamides as activated alkenes and ketones as electrophiles

A simple and convenient protocol for highly diastereoselective intramolecular Baylis-Hillman (IBH) reaction of substrates containing less reactive acrylamides as activated alkene and ketones with α-chiral center (racemic) as electrophile components, thus