71504-00-2

Usage

Uses

Used in Organic Synthesis:
1-(2-BROMO-PHENYL)-3,3-BIS-METHYLSULFANYL-PROPENONE is utilized as a building block in organic synthesis, allowing the creation of more complex molecules. Its unique structure and reactivity make it a valuable component in the synthesis of various organic compounds.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 1-(2-BROMO-PHENYL)-3,3-BIS-METHYLSULFANYL-PROPENONE is used as a key intermediate for the development of new drugs. Its unique properties and reactivity contribute to the design and synthesis of novel pharmaceutical compounds with potential therapeutic applications.
Used in Agrochemicals:
1-(2-BROMO-PHENYL)-3,3-BIS-METHYLSULFANYL-PROPENONE also finds application in the agrochemical sector, where it serves as a starting material for the synthesis of new agrochemicals. Its structure and properties enable the development of innovative products with improved performance in agriculture.
Used in Materials Science:
In the field of materials science, 1-(2-BROMO-PHENYL)-3,3-BIS-METHYLSULFANYL-PROPENONE is employed as a component in the development of advanced materials. Its unique properties and reactivity contribute to the creation of materials with enhanced characteristics for various applications, such as electronics, coatings, and adhesives.

InChI:InChI=1/C11H11BrOS2/c1-14-11(15-2)7-10(13)8-5-3-4-6-9(8)12/h3-7H,1-2H3

Upstream product

• 67-56-1 methanol 
• 1429790-16-8 methyl 3-(2-bromophenyl)-3-oxopropanedithioate 
• 75-15-0 carbon disulfide 
• 2142-69-0 2-bromophenyl methyl ketone 
• 74-88-4 methyl iodide 

Downstream Products

• 1338594-97-0 C₁₉H₁₆BrNO₂ 
• 1338595-03-1 C₁₈H₁₄BrNO₂ 
• 1338595-04-2 (2-bromophenyl)-(4-methanesulfonyl-2,3-dihydro-6H-1-oxa-3a-azaphenalen-5-yl)methanone 
• 1338595-06-4 C₂₄H₁₉BrN₂O₂ 
• 1338595-10-0 C₂₂H₂₃BrN₂O₂ 
• 1338594-90-3 1-(2-bromophenyl)-3-(2,3-dihydrobenzo[1,4]oxazin-4-yl)-3-methylsulfanylpropenone 

Relevant academic research and scientific papers

One-Pot Mitsunobu Protocol to Access Ketene S,S-/N,S-Acetals at Room Temperature

With unique chemical reactivity, α-oxoketene S,S- and N,S-acetals have attracted enormous attention in the past decades, whereas limited reports exist for their synthesis via eco-compatible protocols. Herein, we developed a one-pot protocol for symmetrical and unsymmetrical α-oxoketene S,S-/N,S-acetals through chemoselective alkylation of α-enolic dithioesters using Mitsunobu chemistry at room temperature. The operationally simple and user-friendly mild protocol tolerates a wide range of alcohols and α-enolic dithioesters/β-ketothioamides. Short reaction time, good yields, highly selective C?S functionalization, and E/Z-stereoselectivity are imperative characteristics of this strategy.

Transition metal free synthesis of multifunctional thiomethylated-benzenes from aryl/heteroaryl/cyclopropyl methyl ketones

A base-promoted strategic synthesis of various functionalized thiomethylated-benzenes has been established from aryl/heteroaryl/cyclopropyl methyl ketone. We can directly access the thiomethylated-benzene nucleus embedded with diverse functional group by

Bronsted acid catalyzed PhSe transfer versus radical aryl transfer: Linear codimerization of styrenes and internal olefins

Bronsted acid p-TsOH·H2O-catalyzed hydrovinylation of styrenes with internal olefins α-oxo ketene dithioacetals was efficiently achieved in the presence of N-phenylselenophthalimide (N-PSP), regioselectively affording Markovnikov phenylselenati

Base mediated synthesis of α-aminated aroyl/acetylnaphthalenes through [4+2] annulations

We have developed a base promoted simple, efficient and alternative approach for the synthesis of 4-amino-3-aroyl//heteroaroyl/acetyl-2-methylsulfanyl-naphthalene-1-carbonitriles by reaction of easily accessible 3,3-bis(methylthio)-1-aryl/heteroaryl/acety