76369-25-0

Basic information

• Product Name: 2-Propen-1-one, 1-(4-methoxyphenyl)-3-(methylthio)-3-(phenylamino)-
• CAS NO: 76369-25-0
• Molecular Formula: C17H17NO2S
• Molecular Weight: 299.393
• Mol File: 76369-25-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-Propen-1-one, 1-(4-methoxyphenyl)-3-(methylthio)-3-(phenylamino)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propen-1-one, 1-(4-methoxyphenyl)-3-(methylthio)-3-(phenylamino)-(76369-25-0)
• EPA Substance Registry System: 2-Propen-1-one, 1-(4-methoxyphenyl)-3-(methylthio)-3-(phenylamino)-(76369-25-0)

Safety Data

• Hazardous Substances Data: 76369-25-0(Hazardous Substances Data)

Upstream product

• 33868-76-7 1-(4-methoxyphenyl)-3,3-bis(methylsulfanyl)propenone 
• 62-53-3 aniline 
• 103-72-0 phenyl isothiocyanate 
• 100-06-1 1-(4-methoxyphenyl)ethanone 
• 74-88-4 methyl iodide 

Downstream Products

• 1360604-04-1 3-(4-methoxybenzoyl)-2-phenylamino-4-p-tolyl-4H-pyrano[3,2-c]chromen-5-one 
• 1360604-05-2 3-(4-methoxybenzoyl)-4-(3-nitrophenyl)-2-phenylamino-4H-pyrano[3,2-c]chromen-5-one 
• 1360604-06-3 4-(4-chloro-3-fluorophenyl)-3-(4-methoxybenzoyl)-2-phenylamino-4H-pyrano[3,2-c]chromen-5-one 
• 1619943-16-6 3-(4-methoxybenzoyl)-2-(methylthio)-4-(4-nitrophenyl)-1-phenylpyrrole 
• 1619943-15-5 3-(4-methoxybenzoyl)-2-(methylthio)-1-phenyl-4-(p-tolyl) pyrrole 
• 1619943-14-4 3-(4-methoxybenzoyl)-2-(methylthio)-1,4-diphenylpyrrole 
• 135549-50-7 (6-Chloro-1-phenyl-2-phenylamino-1H-pyrrolo[2,3-b]quinoxalin-3-yl)-(4-methoxy-phenyl)-methanone 
• 135549-48-3 (4-Methoxy-phenyl)-(1-phenyl-2-phenylamino-1H-pyrrolo[2,3-b]quinoxalin-3-yl)-methanone 
• 135549-43-8 4-(4-Methoxy-benzoyl)-1-phenyl-5-phenylamino-1H-pyrrole-2,3-dione 
• 135549-38-1 5-Hydroxy-4-(4-methoxy-benzoyl)-1-phenyl-1H-pyrrole-2,3-dione 
• 81376-46-7 6-(4-Methoxy-phenyl)-1-methyl-2-oxo-4-phenylamino-1,2-dihydro-pyridine-3-carbonitrile 
• 116538-43-3 4-Hydroxy-5-(4-methoxy-benzoyl)-6-methylsulfanyl-1-phenyl-1H-pyridin-2-one 

Relevant articles and documents

ZnCl2-Catalyzed [4+1] Annulation of Alkylthio-Substituted Enaminones and Enaminothiones with Sulfur Ylides

Concise construction of furan and thiophene units has played an important role in the synthesis of potentially bioactive compounds and functional materials. Herein, an efficient Lewis acid ZnCl2 catalyzed [4+1] annulation of alkylthio-substituted enaminones is reported, that is, α-oxo ketene N,S-acetals with sulfur ylides to afford 2-acyl-3-aminofuran derivatives. In a similar fashion, [4+1] annulation of the corresponding enaminothiones, that is, α-thioxo ketene N,S-acetals, with sulfur ylides efficiently proceeded to give multisubstituted 3-aminothiophenes. This method features wide substrate scopes as well as broad functional group tolerance, offering a concise route to highly functionalized furans and thiophenes.

A Novel and Convenient Synthesis of 2-Amino-4-(N-alkyl-N-arylamino)-pyrimidines using Polarized Ketene S,S- and S,N-Acetals

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