41120-12-1

Basic information

• Product Name: 2-[(2-OXO-2-PHENYL-ETHYL)-PHENYL-AMINO]-1-PHENYL-ETHANONE
• Synonyms: 2-[(2-OXO-2-PHENYL-ETHYL)-PHENYL-AMINO]-1-PHENYL-ETHANONE
• CAS NO: 41120-12-1
• Molecular Formula: C₂₂H₁₉NO₂
• Molecular Weight: 329.39
• Mol File: 41120-12-1.mol
• Article Data: 11

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-[(2-OXO-2-PHENYL-ETHYL)-PHENYL-AMINO]-1-PHENYL-ETHANONE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[(2-OXO-2-PHENYL-ETHYL)-PHENYL-AMINO]-1-PHENYL-ETHANONE(41120-12-1)
• EPA Substance Registry System: 2-[(2-OXO-2-PHENYL-ETHYL)-PHENYL-AMINO]-1-PHENYL-ETHANONE(41120-12-1)

Safety Data

• Hazardous Substances Data: 41120-12-1(Hazardous Substances Data)

Usage

Molecular structure

Consists of a phenyl-amino group, a 2-oxo-2-phenyl-ethyl group, and a 1-phenyl-ethanone group.

Type of compound

Ketone, as it contains a carbonyl group (C=O) bonded to two alkyl or aryl groups.

Amine group (-NH2)

The phenyl-amino group indicates the presence of an amine functional group.

Ketone group (C=O)

The 2-oxo-2-phenyl-ethyl group contains a carbonyl group, classifying the compound as a ketone.

Biological activity potential

The presence of both an amine and a ketone suggests that the compound may have biological activity, as these functional groups are commonly found in bioactive molecules.

Specific properties and uses

It is difficult to determine the specific properties and potential uses of this compound without further information.

Upstream product

• 98-86-2 acetophenone 
• 70-11-1 α-bromoacetophenone 
• 62-53-3 aniline 
• 121-69-7 N,N-dimethyl-aniline 
• 5883-81-8 2-anilinoacetophenone 
• 95-92-1 oxalic acid diethyl ester 
• 532-27-4 1-chloroacetophenone 
• 144-62-7 oxalic acid 
• 142-04-1 aniline hydrochloride 
• 540-23-8 p-toluidine hydrochloride 

Downstream Products

• 274690-28-7 1,2,4,6-tetraphenyl-1,4-dihydropyrazine 
• 1393812-12-8 cis-2,4,6-triphenylmorpholine 
• 65-85-0 benzoic acid 
• 26454-88-6 1,4-diphenyl-2-(phenylamino) but-2-ene-1,4-dione 
• 1426307-55-2 [5-chloro-3-(2-fluorophenyl)-1H-2-indolyl](phenyl)methanone 
• 62-53-3 aniline 
• 36004-55-4 (5-chloro-3-phenyl-1H-indol-2-yl)(phenyl)methanone 
• 36004-54-3 phenyl(3-phenyl-1H-indol-2-yl)methanone 
• 5021-43-2 2-phenylquinoxaline 
• 1026148-81-1 2,4,10a-triphenyl-1,10a-dihydro-2H-pyrazino[2,1-b][1,3]benzoxazole 
• 932022-97-4 3,5,7-triphenyl-5,6-dihydro-4H-1,2,5-triazepine 
• 69446-31-7 3,5-diphenyl-5,6-dihydro-1,2,5-oxadiazine 
• 853-36-1 1-(4-methylphenyl)-2,5-diphenylpyrrole 
• 851-33-2 1,2,5-triphenyl-1H-pyrrole 

Relevant articles and documents

A simple and efficient one-step synthesis of 2,4,10a-triaryl-1,10a-dihydro- 2H-pyrazino[2,1-b][1,3] benzothiazoles catalyzed by p-toluene sulfonic acid

A series of 2,4,10a-triaryl-1,10a-dihydro-2H-pyrazino[2,1-b][1,3] benzothiazoles were prepared in good yields by the reaction of 2-[(2-oxo-2-arylethyl) anilino]-1-aryl-1-ethanones with 2-aminothiophenol in the presence of p-toluenesulfonic acid under solv

Synthesis and photochemical properties of 2,4,6,-triaryl-4h-1,4-oxazines

A series of 2,4,6-triaryl-4H-1,4-oxazines was synthesized, and their photochemical properties were studied. The 2,4,6-triaryl-4H-1,4-oxazines underwent photoreaction to N-(1-methoxy-2-oxo-2-arylethyl)-N-arylformamides determined by 1H NMR, 13C NMR, MS, and single crystal X-ray diffraction analyses.

Synthesis of oxathiane and morpholine from acyclic precursors: A modified Mitsunobu reaction

Synthesis of a set of isomeric 2,4,6-triarylmorpholines and 2,6-diaryloxathianes from the corresponding 1,5-diols has been described. The method provides an efficient route to six-membered heterocycles from acyclic diols and is found to be better than Mitsunobu procedure in yield and waste management. In a related study, the ring contraction of pyranone to two isomeric cyclopentenone derivatives through Nazarov reaction has been noticed.