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

General Description

1-(4-CHLORO-PHENYL)-3,3-BIS-METHYLSULFANYL-PROPENONE is an organic compound with the chemical formula C11H11ClOS2. It contains a 4-chlorophenyl group attached to a propenone structure with two methylsulfanyl groups attached to the carbon atom. 1-(4-CHLORO-PHENYL)-3,3-BIS-METHYLSULFANYL-PROPENONE is a yellow solid and is commonly used in organic chemistry as a building block for the synthesis of various pharmaceuticals and agrochemicals. It is also used as an intermediate in the manufacturing of dyes and other organic compounds. Additionally, it has been studied for its potential biological activities and is a known inhibitor of certain enzymes.

Upstream product

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

Downstream Products

• 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 
• 87711-78-2 1-(4-Chloro-phenyl)-3,3-bis-methylsulfanyl-prop-2-en-1-ol 
• 107165-82-2 2-(p-chlorobenzoylmethylene)imidazolidine 
• 124927-51-1 2-(4-chlorobenzoylmethylene)-1-methylimidazolidine 
• 124927-56-6 2-(4-chlorobenzoylmethylene)-1-methylhexahydropyrimidine 
• 201804-49-1 (E)-1-(4-chlorophenyl)-3-methylthio-3-(pyridin-2-ylamino)prop-2-en-1-one 

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.