33046-50-3

Usage

Uses

Used in Pharmaceutical Synthesis:
1-(4-CHLOROPHENYL)-2-[(4-CHLOROPHENYL)SULFANYL]-1-ETHANONE is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drugs with specific therapeutic properties.
Used in Agrochemical Synthesis:
In the agrochemical industry, 1-(4-CHLOROPHENYL)-2-[(4-CHLOROPHENYL)SULFANYL]-1-ETHANONE is utilized as a precursor in the production of agrochemicals, which are essential for enhancing crop protection and yield.
Used in Organic Synthesis:
1-(4-CHLOROPHENYL)-2-[(4-CHLOROPHENYL)SULFANYL]-1-ETHANONE is employed as a reagent in organic synthesis, where its unique structure and reactivity contribute to the creation of a wide range of organic compounds for various applications.
Used in Material Science:
1-(4-CHLOROPHENYL)-2-[(4-CHLOROPHENYL)SULFANYL]-1-ETHANONE is used in material science for its potential to be incorporated into the development of new materials with specific properties, such as improved stability or reactivity.
Used in Chemical Research:
In the field of chemical research, 1-(4-CHLOROPHENYL)-2-[(4-CHLOROPHENYL)SULFANYL]-1-ETHANONE serves as a subject of study for understanding its chemical behavior, reactivity, and potential applications in creating new compounds and materials.

InChI:InChI=1/C14H10Cl2OS/c15-11-3-1-10(2-4-11)14(17)9-18-13-7-5-12(16)6-8-13/h1-8H,9H2

Upstream product

• 106-54-7 p-Chlorothiophenol 
• 873-73-4 4-n-chlorophenylacetylene 
• 536-38-9 4-chlorobenzoylmethyl bromide 

Downstream Products

• 1330539-97-3 C₂₀H₁₂Cl₃NS 
• 1330539-93-9 C₂₀H₁₃Cl₂NS 
• 1330540-13-0 3-(4-chlorophenylsulfonyl)-2-(4-chlorophenyl)-1H-indole 
• 1260255-26-2 1-(4-chlorophenyl)-2-[(4-chlorophenyl)sulfanyl]-1-ethanone N-(Z)-1-(4-chlorophenyl)-2-[(4-chlorophenyl)sulfanyl]ethylidenehydrazone 
• 1235497-43-4 6-(4-chlorophenyl)-5-[(4-chlorophenyl)sulfanyl]-2-ethoxy-4-phenylnicotinonitrile 
• 1235497-56-9 4,6-bis(4-chlorophenyl)-5-[(4-chlorophenyl)sulfanyl]-2-methoxynicotinonitrile 
• 19968-41-3 4-(4-chloro-phenyl)-5-(4-chloro-phenylsulfanyl)-3H-thiazol-2-one 

Relevant academic research and scientific papers

Electrocatalytic Synthesis of gem -Bisarylthio Enamines and α-Phenylthio Ketones via a Radical Process under Mild Conditions

The novel method for the synthesis of gem -bisarylthio enamines and α-phenylthio ketones was developed via the coupling of α-substituted vinyl azides with thiols in the presence of tetrabutylammonium iodide (TBAI) as a redox catalyst and electrolyte at ro

Unprecedented C-2 arylation of indole with diazonium salts: Syntheses of 2,3-disubstituted indoles and their antimicrobial activity

A novel reaction of indole with aryldiazonium salts leading to the formation of 2-aryl-3-(arylazo)indoles was discovered. The products were found to possess potent anti-MRSA and anti-LLVRE activities. The SAR studies indicate that the potentially metaboli

Selective one-pot multicomponent synthesis and anti-tubercular evaluation of 5-(aryl/cyclohexylsulfanyl)-2-alkoxy-4,6-diarylnicotinonitriles

A new set of highly substituted pyridine derivatives has been synthesized by a product selective four component reaction of aryl aldehyde, malononitrile and 2-aryl/cyclohexylsulfanyl-1-aryl-1-ethanones in presence of sodium hydroxide in methyl/ethyl alcoh

Pyrazole derivatives from azines of substituted phenacyl aryl/cyclohexyl sulfides and their antimycobacterial activity

Azines derived from substituted phenacyl aryl/cyclohexyl sulfide on treatment with excess phosphorous oxychloride in N,N-dimethylformamide have been found to yield two isomeric pyrazoles in each case. A plausible mechanism has been suggested for the forma

Structure-activity relationship of antileishmanials neolignan analogues

Twenty-two synthetic analogues of neolignans comprising β-ketoethers and β-ketosulfides were obtained from condensation reactions among β-bromoketones and phenols or thiophenols, respectively, in basic solutions, and assayed in vitro for activity against