134129-19-4

Basic information

• Product Name: Benzenepropanal, a-[bis(methylthio)methylene]-b-oxo-
• CAS NO: 134129-19-4
• Molecular Formula: C12H12O2S2
• Molecular Weight: 252.358
• Mol File: 134129-19-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzenepropanal, a-[bis(methylthio)methylene]-b-oxo-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenepropanal, a-[bis(methylthio)methylene]-b-oxo-(134129-19-4)
• EPA Substance Registry System: Benzenepropanal, a-[bis(methylthio)methylene]-b-oxo-(134129-19-4)

Safety Data

• Hazardous Substances Data: 134129-19-4(Hazardous Substances Data)

Upstream product

• 13636-88-9 3,3-bis(methylthio)-1-phenylprop-2-en-1-one 
• 68-12-2 N,N-dimethyl-formamide 
• 75-15-0 carbon disulfide 
• 41125-10-4 benzoylacetaldehyde sodium salt 
• 74-88-4 methyl iodide 

Downstream Products

• 1639452-84-8 3-amino-2-benzoyl-3-(methylsulfanyl)-2-propenal 
• 931114-31-7 (5-amino-1H-pyrazol-4-yl)(phenyl)methanone 
• 34631-59-9 (E)-2-(bis(methylthio)methylene)-1,4-diphenylbut-3-en-1-one 
• 1059605-73-0 (2-(methylthio)-5-phenylfuran-3-yl)(phenyl)methanone 
• 1099823-58-1 3-(methylsulfanyl)-5-phenyl-4-isoxazolecarbaldehyde oxime 
• 1099823-51-4 [5-(methylsulfanyl)-4-isoxazolyl](phenyl)methanone 
• 68364-88-5 3-(methylsulfanyl)-5-phenyl-4-isoxazolecarbonitrile 
• 881889-90-3 2-[2-benzoyl-3,3-bis(methylsulfanyl)-2-propenylidene]malononitrile 
• 13636-88-9 3,3-bis(methylthio)-1-phenylprop-2-en-1-one 

Relevant articles and documents

The reaction of 2-aroyl-3,3-bis(alkylsulfanyl)acrylaldehydes and hydroxylamine hydrochloride: Facile synthesis of differently substituted isoxazoles

(Chemical Equation Presented) 2-Aroyl-3,3-bis(alkylsulfanyl)acrylaldehyde was utilized for the synthesis of three different isoxazoles by reacting with hydroxylaminehydrochloride. We synthesized differently substituted isoxazoles like (aryl)[5-(methylsulf

A convenient preparation of 2-aroyl-3,3-bis(alkylsulfanyl)acrylaldehydes and their application in the synthesis of 5-aroyl-2-oxo-1,2-dihydro-2- pyridinecarbonitriles

The reaction of aroylketene dithioacetals 1 with Vilsmeier-Haack reagent, prepared from POCl3 and DMF, under mild conditions gave 2-aroyl-3,3-bis(alkylsulfanyl)acrylaldehydes 2 in excellent yields. Cyclization of 2-[2-aroyl-3,3-bis(methylsulfan