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2-(4-methoxyphenyl)-1-phenyl-2-(phenylamino)ethanone is a complex organic compound with the molecular formula C25H23NO2. It is a derivative of acetophenone, featuring a phenyl group attached to the carbonyl carbon, a 4-methoxyphenyl group on the adjacent carbon, and a phenylamino group on the terminal carbon. 2-(4-methoxyphenyl)-1-phenyl-2-(phenylamino)ethanone is characterized by its aromatic structure and the presence of an amide-like linkage due to the phenylamino group. It is likely to be used in the synthesis of various pharmaceuticals, dyes, or other organic compounds due to its versatile functional groups. The compound's properties, such as solubility and reactivity, can be influenced by the electron-donating methoxy group and the electron-rich phenyl rings, making it a potentially interesting molecule for further chemical exploration and application.

6338-31-4

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6338-31-4 Usage

Chemical structure

2-(4-methoxyphenyl)-1-phenyl-2-(phenylamino)ethanone is a complex compound containing a methoxyphenyl group, a phenyl group, and a phenylamino group.

Classification

It is classified as an ethanone, which is a type of ketone compound.

Usage

Commonly used in organic synthesis and medicinal chemistry.

Applications

Often used as an intermediate in the production of pharmaceuticals and agrochemicals.

Versatility

Unique structure makes it a versatile building block for the creation of new compounds with various biological and chemical properties.

Safety precautions

Due to its complex structure and potential reactivity, careful handling and proper safety precautions are necessary when working with 2-(4-methoxyphenyl)-1-phenyl-2-(phenylamino)ethanone.

Check Digit Verification of cas no

The CAS Registry Mumber 6338-31-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,3 and 8 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6338-31:
(6*6)+(5*3)+(4*3)+(3*8)+(2*3)+(1*1)=94
94 % 10 = 4
So 6338-31-4 is a valid CAS Registry Number.

6338-31-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-anilino-2-(4-methoxyphenyl)-1-phenylethanone

1.2 Other means of identification

Product number -
Other names 4'-Methoxy-desylanilin

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6338-31-4 SDS

6338-31-4Relevant academic research and scientific papers

Visible-Light-Induced Radical Acylation of Imines with α-Ketoacids Enabled by Electron-Donor-Acceptor Complexes

Zhang, Hong-Hao,Yu, Shouyun

supporting information, p. 3711 - 3715 (2019/05/24)

A visible-light-induced radical acylation of imines with α-ketoacids has been achieved, enabled by an electron-donor-acceptor (EDA) complex. This EDA complex-mediated process eradicates the use of a photocatalyst. Visible light is used as the sole promote

Titanium-mediated reductive cross-coupling reactions of imines with nitriles: An efficient route for the synthesis of α-aminoketones or 1,2-diketones

Chen, Haoyi,Fan, Guoqin,Li, Shi,Mao, Kebin,Liu, Yuanhong

supporting information, p. 1593 - 1596 (2014/03/21)

The reaction of imines with low-valent titanium species, generated in situ by using Ti(OiPr)4/2 c-C5H9MgCl reagent, affords titanium-imine complex, which can couple with nitriles to provide 2,5-diazatitanacyclop

Highly stereoselective synthesis of β-amino ketones via a mannich reaction catalyzed by cellulose sulfuric acid as a biodegradable, efficient, and recyclable heterogeneous catalyst

Nemati, Firouzeh,Fakhaei, Amir Soheyl,Amoozadeh, Ali,Hayeniaz, Yaser Saeidi

experimental part, p. 3695 - 3702 (2011/10/09)

The efficient use of cellulose sulfuric acid as a heterogeneous catalyst promotes three-component, one-pot Mannich reaction of various ketones, aromatic aldehydes, and aromatic amines in ethanol to make the corresponding β-amino ketones with high stereose

Thiazolium-derived N-heterocyclic carbene-catalyzed cross-coupling of aldehydes with unactivated imines

Li, Gong-Qiang,Dai, Li-Xin,You, Shu-Li

, p. 852 - 854 (2007/10/03)

Cross-coupling of aromatic aldehydes or benzoins with unactivated imines catalyzed by an N-heterocyclic carbene (NHC) affords α-amino ketones smoothly. The Royal Society of Chemistry.

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