4198-95-2

Basic information

• Product Name: (2E)-1,2-diphenyl-2-(phenylimino)ethanone
• Synonyms: (2E)-1,2-Diphenyl-2-(phenylimino)ethanone; Ethanone, diphenyl(phenylimino)-
• CAS NO: 4198-95-2
• Molecular Formula: C₂₀H₁₅NO
• Molecular Weight: 285.3392
• Mol File: 4198-95-2.mol
• Article Data: 13

Chemical Properties

• Boiling Point: 441.5°C at 760 mmHg
• Flash Point: 182.2°C
• Density: 1.05g/cm³
• Vapor Pressure: 5.43E-08mmHg at 25°C
• Refractive Index: 1.586
• CAS DataBase Reference: (2E)-1,2-diphenyl-2-(phenylimino)ethanone(CAS DataBase Reference)
• NIST Chemistry Reference: (2E)-1,2-diphenyl-2-(phenylimino)ethanone(4198-95-2)
• EPA Substance Registry System: (2E)-1,2-diphenyl-2-(phenylimino)ethanone(4198-95-2)

Safety Data

• Hazardous Substances Data: 4198-95-2(Hazardous Substances Data)

Usage

Description

(2E)-1,2-diphenyl-2-(phenylimino)ethanone is a chemical compound belonging to the class of imines, characterized by a double bond between carbon and nitrogen. It has a molecular formula of C20H15NO, a yellow solid appearance, and a molecular weight of 281.34 g/mol.

Uses

Used in Organic Synthesis:
(2E)-1,2-diphenyl-2-(phenylimino)ethanone is used as a building block in organic synthesis for the creation of a variety of compounds. Its unique structure allows it to be a versatile component in the synthesis of complex organic molecules.
Used in Pharmaceutical Research:
In pharmaceutical research, (2E)-1,2-diphenyl-2-(phenylimino)ethanone is utilized as a starting material for the development of new drugs. Its pharmacological activities and potential therapeutic effects make it a valuable candidate for further investigation and application in medicinal chemistry.
Used in Chemical Education:
Due to its distinctive properties and reactivity, (2E)-1,2-diphenyl-2-(phenylimino)ethanone can be employed as an educational tool in chemistry courses to illustrate concepts related to imine chemistry and organic synthesis.
Safety Note:
It is crucial to handle (2E)-1,2-diphenyl-2-(phenylimino)ethanone with care, as it may have potential risks to health and the environment. Proper safety measures and disposal methods should be followed to mitigate any adverse effects.

Upstream product

• 5722-91-8 1,2-diphenyl-2-(phenylamino)ethanone 
• 121-69-7 N,N-dimethyl-aniline 
• 62-53-3 aniline 
• 71-43-2 benzene 
• 103-71-9 phenyl isocyanate 
• 134-81-6 benzil 
• 134225-83-5 1-Hydroxy-2--1,2-diphenylethyl diphenylphosphinodithioate 
• 20732-26-7 lithium anilide 
• 861566-69-0 4,5-dihydroxy-1,3,4,5-tetraphenyl-imidazolidin-2-one 
• 108-24-7 acetic anhydride 
• 4746-86-5 hydroxy-diphenyl-acetaldehyde 
• 100-52-7 benzaldehyde 
• 588-59-0 stilbene 
• 63369-91-5 α-chloro-α-(chlorosulfenyl)benzyl phenyl ketone 

Downstream Products

• 60036-63-7 (+/-)-2-hydroxy-1.2-diphenyl-propanone-⁽¹⁾-phenylimine 
• 5722-91-8 1,2-diphenyl-2-(phenylamino)ethanone 
• 82940-37-2 erythro-2-(N-phenylamino)-1,2-diphenylethanol 
• 1922-78-7 anilino-diphenyl-acetic acid 
• 76-93-7 Benzilic acid 
• 7510-33-0 N,N'-diphenyl-1,2-diphenylethane-1,2-diimine 
• 87277-36-9 [3-(4-Chloro-phenyl)-4,5-diphenyl-4,5-dihydro-[1,2,4]oxadiazol-5-yl]-phenyl-methanone 
• 97531-36-7 2-Ethoxy-3,4,5-triphenyl-3H-[1,3,2]oxazaphosphole 2-sulfide 
• 80783-92-2 N-(2-Oxo-1,2-diphenyl-ethyl)-N-phenyl-propionamide 
• 84197-54-6 4-Benzoyl-3-methyl-1,4-diphenyl-azetidin-2-one 
• 139696-56-3 2-Methoxy-2-methyl-3,4,5-triphenyl-2,3-dihydro-[1,3,2]oxazasilole 
• 87277-25-6 Phenyl-(3,4,5-triphenyl-4,5-dihydro-[1,2,4]oxadiazol-5-yl)-methanone 
• 84197-57-9 4-Benzoyl-1,3,4-triphenyl-azetidin-2-one 
• 69085-78-5 3,4,5-triphenyl-2-phenyliminooxazoline 

Relevant articles and documents

High norbornene incorporation in ethylene-norbornene copolymerization with a bis(α-alkyloxoimine) titanium-MAO catalyst

A novel bis(α-alkyloxoimine) titanium(IV) complex was synthesized and used as a catalyst precursor to catalyze homo-and copolymerization of ethylene and norbornene. The titanium complex activated with methylalumoxane exhibits good activities for the homopolymerizations of ethylene and norbornene under high temperature to produce high-molecular-weight linear polyethylene and vinyl-type polynorbornene, respectively. Ethylene-norbornene copolymers with high molecular weight can also be produced by this catalyst. The incorporation of norbornene from 0 to 76 mol% in the copolymers can be controlled by varying the charged norbornene. 13C NMR analyses show that the microstructures of the ethylene-norbornene copolymers with low norbornene incorporation are predominantly alternated and isolated norbornene units, while those with high norbornene incorporation are random polymers containing long norbornene sequences. Science China Press and Springer-Verlag Berlin Heidelberg 2010.

Selective synthesis of 1,4,5-trisubstituted imidazoles from α-imino ketones prepared by N-heterocyclic-carbene-catalyzed aroylation

An alternative synthetic route to 1,4,5-trisubstituted imidazoles from α-imino ketone, which can be prepared from imidoyl chlorides and aromatic aldehydes via N-heterocycle carbene-catalyzed aroylation was developed. This methodology consists of simple tr

Synthesis and characterization of 9,10-bis(arylimino)-9,10-dihydrophenanthrenes, the structure of (Z,Z)-9,10-bis(phenylimino)-9,10-dihydrophenanthrene and PdCl2-[(E,E)-9,10-bis(phenylimino)-9,10-dihydrophenanthrene] in the solid state and in so

The synthesis and characterization of substituted phenanthrene-9,10-quinone diimines of the type 9,10-bis(arylimino)-9,10-dihydrophenanthrene (aryl-BIP) is described. These rigid bisnitrogen ligands have been synthesized by a metal-mediated cyclodehydroge