35755-44-3

Usage

Uses

Used in Plastics Industry:
1-(4-chlorophenyl)-2-[(4-chlorophenyl)amino]ethanone is used as a UV absorber for [application reason] protecting plastics from the degrading effects of ultraviolet radiation, thereby enhancing their durability and longevity.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 1-(4-chlorophenyl)-2-[(4-chlorophenyl)amino]ethanone serves as an intermediate in the synthesis of various pharmaceuticals, contributing to the development of new drugs and medicines.
Used in Dye Industry:
1-(4-chlorophenyl)-2-[(4-chlorophenyl)amino]ethanone is utilized as a reactive dye intermediate, playing a crucial role in the production of dyes that are used in different applications, including textiles and other industrial processes.
Used in Organic Chemistry:
As a building block, 1-(4-chlorophenyl)-2-[(4-chlorophenyl)amino]ethanone is employed in the production of other organic compounds, showcasing its versatility and importance in the field of organic chemistry.

Upstream product

• 106-47-8 4-chloro-aniline 
• 115400-12-9 p-chlorophenacyl benzenesulphonate 
• 118985-11-8 p-chlorophenacyl p-chlorobenzenesulphonate 
• 118985-12-9 p-chlorophenacyl m-nitrobenzenesulphonate 
• 536-38-9 4-chlorobenzoylmethyl bromide 
• 99-91-2 para-chloroacetophenone 
• 25917-49-1 1-(4-chlorophenyl)-2-(p-tolylsulfonyloxy)ethanone 

Downstream Products

• 146537-29-3 ethyl 1,4-bis(4-chlorophenyl)-2-methyl-1H-pyrrole-3-carboxylate 
• 705972-09-4 N₁-(4-chlorophenyl)-N₁-[2-(4-chlorophenyl)-2-oxoethyl]-2-phenylacetamide 
• 256331-94-9 1,4-bis(4-chlorophenyl)-2-(dimethylamino)-1H-imidazole 
• 256332-25-9 1,4-bis(4-chlorophenyl)-2-(dimethylamino)-1H-imidazole-5-carbaldehyde 
• 1443130-47-9 (4-chlorophenyl)(3-(4-chlorophenyl)-1-p-tolylimidazolidin-4-yl)methanone 
• 1443130-48-0 (4-Chlorophenyl)(3-(4-chlorophenyl)-1-(4-methoxyphenyl)imidazolidin-4-yl)methanone 

Relevant academic research and scientific papers

A one-pot and three-component synthetic approach for the preparation of asymmetric and multi-substituted 1,4-dihydropyrazines

An efficient, one-pot and three-component synthesis of a new series of 2-acyl-3,4,6-triaryl-1,4-dihydropyrazines is described. This two-step strategy involves treatment of phenacyl bromides and anilines to give the nucleophilic substitution intermediate f

New efficient synthesis of 1,4-benzodiazepin-5-ones by catalytic aza-Wittig reaction

1,4-Benzodiazepin-5-ones were synthesized in 71-89% yields from 2-isocyanato-N-(2-oxoalkyl)benzamides via a new catalytic intramolecular aza-Wittig reaction. Starting from easily accessible phthalic anhydride and α-arylamino ketones, the corresponding 2-{[(2-oxoalkyl)amino]carbonyl}benzoic acids underwent sequential formation of the acid azide and Curtis rearrangement to give 2-isocyanato-N-(2-oxoalkyl)benzamides that were reacted directly to give the final 2,4-diaryl-3,4-dihydro-5H-1,4-benzodiazepin-5-ones and 4-aryl-2-tert-butyl-3,4-dihydro-5H-1,4-benzodiazepin-5-ones.

Synthesis, Characterization, and Antibacterial Activity of Some Novel Substituted Imidazole Derivatives via One-pot Three-Component

A simple and highly efficient one-pot, three-component synthesis of novel substituted imidazole derivatives has been reported by the reaction of 3-(2-bromoacetyl)-2H-chromen-2-one, ammonium thiocyanate, and phenacyl aniline in the presence of acetic acid

Synthesis, antibacterial activity and binding mode analysis of some novel 1,4-diaryl imidazole thiones

A novel series of fifteen diaryl imidazole thiones 2a-o was synthesized by reacting the corresponding 1-(aryl)-2-(arylamino)-ethanones 1 with ammonium thiocyanate. The compounds have been characterized on the basis of elemental analysis and spectral data.

A rapid and direct access to symmetrical/unsymmetrical 3,4-diarylmaleimides and pyrrolin-2-ones

1,8-Diazabicyclo[5.4.0]undec-7ene (DBU) facilitated the oxidative cyclization of phenacyl amide in the presence of atmospheric oxygen under environmentally friendly conditions. The reaction has been studied under various conditions and a plausible mechani

Hypervalent iodine mediated syntheses of heterocycles: One-pot facile syntheses of 1,4-diaryl-2-mercaptoimidazoles, 2-(α-anilinoacetyl)thiophenes and 1-aryl-2-mercapto-4-(2-thienyl)imidazoles from aryl/2-thienyl methyl ketones

Successive treatment of acetophenones (1a-e) or 2-acetylthiophene (4) with benzene, appropriate aniline and KSCN/AcOH leads to the formation of 1,4-diaryl-2-mercaptoimidazoles (3aa-3ea) or 1-aryl-2-mercapto-4-(2-thienyl)imidazoles (6a-f) respectively.This procedure also provides 2(α-anilinoacetyl)thiophenes (5a-f) in one pot from 4.

Research on antibacterial and antifungal agents. VIII. Synthesis and antimicrobial activity of 1,4-diarylpyrroles

The synthesis and the antimicrobial activity of 1,4-diarylpyrroles are reported. The obtained data in comparison with pyrrolnitrin show that many acid derivatives 4 exhibit a selective activity against some strains of Candida spp and poor activity against

Nucleophilic Substitution Reactions of Phenacyl Benzenesulphonates with Anilines in Methanol-Acetonitrile Mixtures

The nucleophilic substitution reactions of phenacyl benzenesulphonates with anilines in methanol-acetonitrile have been studied.A stronger nucleophile was found to cause less bond cleavage, while a better leaving group led to less bond formation, in compl