742-43-8

Basic information

• Product Name: 1-Propanone, 1,3-diphenyl-3-(phenylamino)-
• CAS NO: 742-43-8
• Molecular Formula: C21H19NO
• Molecular Weight: 301.388
• Mol File: 742-43-8.mol
• Article Data: 157

Chemical Properties

• CAS DataBase Reference: 1-Propanone, 1,3-diphenyl-3-(phenylamino)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Propanone, 1,3-diphenyl-3-(phenylamino)-(742-43-8)
• EPA Substance Registry System: 1-Propanone, 1,3-diphenyl-3-(phenylamino)-(742-43-8)

Safety Data

• Hazardous Substances Data: 742-43-8(Hazardous Substances Data)

Usage

Class

Aromatic ketones

Physical state

Yellow crystalline solid

Common uses

Intermediate in the synthesis of pharmaceuticals and other organic compounds

Industrial applications

Building block in the production of perfumes, organic pigments, and dyes

Medicinal properties

Tyrosine kinase inhibitor, potential use in cancer research

Additional properties

Mild antibiotic and antifungal activities

Upstream product

• 62-53-3 aniline 
• 614-47-1 1,3-diphenyl-propen-3-one 
• 100-52-7 benzaldehyde 
• 98-86-2 acetophenone 
• 100-51-6 benzyl alcohol 
• 536-74-3 phenylacetylene 
• 100-61-8 N-methylaniline 
• 75-04-7 ethylamine 
• 13735-81-4 1-styrenyloxytrimethylsilane 
• 538-51-2 benzylidene phenylamine 
• 104-88-1 4-chlorobenzaldehyde 
• 70-11-1 α-bromoacetophenone 
• 1750-36-3 (E)-N-benzylidenebenzenamine 
• 71115-31-6 3-imino-1,3,N-triphenylprop-1-enylamine 

Downstream Products

• 94-41-7 benzalacetophenone 
• 614-47-1 1,3-diphenyl-propen-3-one 
• 63255-41-4 1,3-diphenyl-3-phenylaminopropenone 
• 874131-13-2 (R)-1,3-diphenyl-3-(N-phenylamino)propan-1-one 
• 1092456-76-2 (S)-1,3-diphenyl-3-(phenylamino)propan-1-one 
• 1612152-86-9 3-(diphenylamino)-1,3-diphenylpropan-1-one 
• 6049-56-5 N-Phenyl-β-phenyl-β-alanine 
• 61484-75-1 β-Phenyl-β'-anilinopropionsaeureanilid 
• 6846-55-5 ethyl 3-anilino-3-phenylpropanoate 
• 95003-25-1 C₂₁H₂₀N₂O 
• 175350-44-4 4-benzoyl-1,5-diphenyl-pyrrolidine-2,3-dione 
• 4566-58-9 (1R,3R)-1,3-Diphenyl-3-phenylamino-propan-1-ol 
• 4566-58-9 erythro-3-Anilino-1,3-diphenyl-propanol 
• 77670-30-5 diethyl 2-(3-oxo-1,3-diphenylpropyl)malonate 

Relevant articles and documents

Ln(OTf)3- or Cu(OTf)2-catalyzed Mannich-type reactions of aldehydes, amines, and silyl enolates in micellar systems. Facile synthesis of β-amino ketones and esters in water

In the presence of a catalytic amount of Ln(OTf)3 or Cu(OTf)2, three- component Mannich-type reactions of aldehydes, amines, and silyl enolates proceeded smoothly in micellar systems to afford the corresponding β-amino ketones or est

Air-stable Organoantimony (III) Perfluoroalkyl(aryl)sulfonate complexes as highly efficient, selective, and recyclable catalysts for C–C and C–N bond-forming reactions

A series of air-stable organoantimony (III) perfluoroalkyl(aryl)sulfonate complexes with an azastibocine framework {t-BuN(CH2C6H4)2SbOSO2C4F9 (2a); [t-BuN(CH2C6/

A ZnS@N-GQD nanocomposite as a highly effective and easily retrievable catalyst for the sonosynthesis of β-amino carbonyls

A three-component reaction of acetophenone, aromatic aldehydes, and aniline derivatives has been achieved in the presence of a ZnS@nitrogen graphene quantum dot (N-GQD) nanocomposite as a highly effective heterogeneous catalyst to produce β-amino carbonyls. The catalyst has been characterized by XRD, SEM, TEM, FT-IR spectroscopy, EDS, BET and TGA techniques. The feasibility of carrying out the one-pot synthesis under ultrasonic irradiation with a heterogeneous nanocatalyst could improve the reaction rates and shorten the reaction times.