95005-60-0

Basic information

• Product Name: 3-(N-p-chlorophenylamino)-2-methyl-1,3-diphenyl-1-propanone
• Synonyms: 3-(N-p-chlorophenylamino)-2-methyl-1,3-diphenyl-1-propanone
• CAS NO: 95005-60-0
• Molecular Weight: 349.86
• Mol File: 95005-60-0.mol

Chemical Properties

• CAS DataBase Reference: 3-(N-p-chlorophenylamino)-2-methyl-1,3-diphenyl-1-propanone(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(N-p-chlorophenylamino)-2-methyl-1,3-diphenyl-1-propanone(95005-60-0)
• EPA Substance Registry System: 3-(N-p-chlorophenylamino)-2-methyl-1,3-diphenyl-1-propanone(95005-60-0)

Safety Data

• Hazardous Substances Data: 95005-60-0(Hazardous Substances Data)

Upstream product

• 66323-99-7 trimethyl[(Z)-(1-phenyl-1-propenyl)oxy]silane 
• 780-21-2 N-(4-chlorobenzylidene)aniline 
• 100-52-7 benzaldehyde 
• 106-47-8 4-chloro-aniline 
• 93-55-0 1-phenyl-propan-1-one 
• 1613-89-4 (E)-N-benzylidene-4-chloroaniline 

Relevant articles and documents

Mannich-Type Reactions of Aldehydes, Amines, and Ketones in a Colloidal Dispersion System Created by a Bronsted Acid-Surfactant-Combined Catalyst in Water

(matrix presented) Three-component Mannich-type reactions of aldehydes, amines, and ketones were efficiently catalyzed by dodecylbenzenesulfonic acid at ambient temperature in water to give various β-amino ketones in good yields. The same reactions proceeded sluggishly in organic solvents.

Mannich-type reactions of aromatic aldehydes, anilines, and methyl ketones in fluorous biphase systems created by rare earth (III) perfluorooctane sulfonates catalysts in fluorous media

Rare earth (III) perfluorooctane sulfonates (RE(OPf)3) catalyze the three-component Mannich-type reactions of different ketones with various aromatic aldehydes and aromatic amines in fluorous media to give various β-arylamino ketones in good yields. By simple separation of the fluorous phase containing only catalyst, reaction can be repeated several times.

Three-component carbon-carbon bond-forming reactions catalyzed by a Br?nsted acid-surfactant-combined catalyst in water

Reactions of aldehydes, amines, and various nucleophiles such as silyl enolates, ketones, Danishefsky's diene, and allyltribuyltin in water were successfully carried out in the presence of p-dodecylbenzenesulfonic acid (DBSA) as a Br?nsted acid-surfactant-combined catalyst.

Aldehydes vs aldimines. Unprecedented aldimine-selective nucleophilic additions in the coexistence of aldehydes using a lanthanide salt as a Lewis acid catalyst

It is well-recognized that aldimines are less reactive than aldehydes toward nucleophilic additions. In this paper, an unprecedented change in the reactivity is described: preferential reactions of aldimines over aldehydes in nucleophilic additions using