41467-26-9

Basic information

• Product Name: 1-(4-CHLORO-PHENYL)-3,3-BIS-METHYLSULFANYL-PROPENONE
• Synonyms: 1-(4-CHLORO-PHENYL)-3,3-BIS-METHYLSULFANYL-PROPENONE;1-(4-Chlorophenyl)-3,3-bis(methylthio)prop-2-en-1-one;1-(4-chlorophenyl)-3,3-bis(methylsulfanyl)prop-2-en-1-one
• CAS NO: 41467-26-9
• Molecular Formula: C₁₁H₁₁ClOS₂
• Molecular Weight: 259.79538
• Mol File: 41467-26-9.mol
• Article Data: 20

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-(4-CHLORO-PHENYL)-3,3-BIS-METHYLSULFANYL-PROPENONE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-CHLORO-PHENYL)-3,3-BIS-METHYLSULFANYL-PROPENONE(41467-26-9)
• EPA Substance Registry System: 1-(4-CHLORO-PHENYL)-3,3-BIS-METHYLSULFANYL-PROPENONE(41467-26-9)

Safety Data

• Hazardous Substances Data: 41467-26-9(Hazardous Substances Data)

Usage

Description

1-(4-CHLORO-PHENYL)-3,3-BIS-METHYLSULFANYL-PROPENONE, an organic compound with the chemical formula C11H11ClOS2, is a yellow solid featuring a 4-chlorophenyl group attached to a propenone structure, with two methylsulfanyl groups connected to the carbon atom. 1-(4-CHLORO-PHENYL)-3,3-BIS-METHYLSULFANYL-PROPENONE is recognized for its versatile applications in the synthesis of pharmaceuticals, agrochemicals, dyes, and other organic compounds, as well as its potential biological activities and enzyme-inhibiting properties.

Uses

Used in Pharmaceutical Industry:
1-(4-CHLORO-PHENYL)-3,3-BIS-METHYLSULFANYL-PROPENONE is used as a building block for the synthesis of various pharmaceuticals due to its unique chemical structure and reactivity, contributing to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, 1-(4-CHLORO-PHENYL)-3,3-BIS-METHYLSULFANYL-PROPENONE serves as an intermediate for the production of agrochemicals, such as pesticides and herbicides, leveraging its chemical properties to enhance the effectiveness of these products.
Used in Dye Manufacturing:
1-(4-CHLORO-PHENYL)-3,3-BIS-METHYLSULFANYL-PROPENONE is used as an intermediate in the manufacturing of dyes, where its chemical composition plays a crucial role in the development of new dye formulations with improved color properties and stability.
Used in Organic Chemistry Research:
As a compound with potential biological activities, 1-(4-CHLORO-PHENYL)-3,3-BIS-METHYLSULFANYL-PROPENONE is utilized in organic chemistry research for studying its interactions with various enzymes, aiming to discover new applications in the field of biochemistry and drug development.

Upstream product

• 50850-04-9 1-(4-chlorophenyl)-3,3-dimercapto-2-propen-1-one 
• 74-88-4 methyl iodide 
• 75-15-0 carbon disulfide 
• 74-83-9 methyl bromide 
• 99-91-2 para-chloroacetophenone 
• 77-78-1 dimethyl sulfate 

Downstream Products

• 50267-88-4 (Z)-3-(4-chloro-phenyl)-3-methylsulfanyl-dithioacrylic acid methyl ester 
• 76369-36-3 4-(4-Chloro-phenyl)-6-morpholin-4-yl-pyrimidin-2-ylamine 
• 123559-07-9 2-(4-Chloro-phenyl)-4,4-bis-methylsulfanyl-but-3-en-2-ol 
• 90254-55-0 7-(p-chlorophenyl)-1,3-dimethyl-5-methylthiopyrido<2,3-d>pyrimidine-2,4(1H,3H)-dione 
• 130001-05-7 (E)-2-<(4-chlorpbenzoyl)methylene>-5,5-dimethyl-tetrahydro-2H-1,3-oxazine 
• 74-93-1 methylthiol 
• 126232-72-2 (R)-(-)-(E)-2-<(4-chlorobenzoyl)methylene>-4-ethyl-2-oxazolidine 
• 82754-46-9 E-3-Methylthio-1-(4-chlorophenyl)-2-propen-1-one 
• 140611-71-8 2-Acetoxy-3,3-bis(methylthio)-1-(4-chlorophenyl)-2-propen-1-one 
• 140611-76-3 1,6-Di(4-chlorophenyl)-3,3,4,4-tetra(methylthio)hexane-1,2,5,6-tetraone 
• 98606-78-1 2-bromo-1-(4-chlorophenyl)-3,3-bis(methylthio)prop-2-en-1-one 
• 120803-16-9 5-(4-chlorophenyl)-3-(methylthio)isoxazole 
• 120803-07-8 3-(4-chlorophenyl)-5-methylthio-isoxazole 
• 116991-69-6 (4-Chloro-phenyl)-(5-methylsulfanyl-1H-[1,2,3]triazol-4-yl)-methanone 

Relevant articles and documents

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

Synthesis of Partially Reduced Imidazo[1,2- a ]pyridines through an Unprecedented Base-Mediated (4+2) Cyclization

A water-mediated regioselective synthesis of 6,7-diaryl-5-oxo-2,3,5,6-tetrahydroimidazo[1,2-a]pyridine-6-carbonitriles was performed by the reaction of 2-[1-cyano-2,2-bis(methylsulfanyl)vinyl]benzonitrile with 1-aryl-2-(imidazolidin-2-ylidene)ethanones un

Synthesis of β-amino-α,β-unsaturated ketone derivatives via sequential rhodium-catalyzed sulfur ylide formation/rearrangement

In the presence of a Rh(II) catalyst and β-(methylthio)-α,β-unsaturated ketones, 1-sulfonyl-1,2,3-triazoles can be converted into functionalized β-amino-α,β-unsaturated ketones via formation of α-imino rhodium carbene/sulfur ylide and subsequent rearrangement. The products decompose to useful 2-methylthiopyrrole derivatives conveniently in high yield.