121654-79-3

Basic information

• Product Name: 2-(cyclohexylcarbonyl)-4-thioxo-1,2,3,4,6,7,8,12b-octahydropyrazino<2,1-a><2>benzazepine
• Synonyms: 2-(cyclohexylcarbonyl)-4-thioxo-1,2,3,4,6,7,8,12b-octahydropyrazino<2,1-a><2>benzazepine
• CAS NO: 121654-79-3
• Molecular Weight: 342.505
• Mol File: 121654-79-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-(cyclohexylcarbonyl)-4-thioxo-1,2,3,4,6,7,8,12b-octahydropyrazino<2,1-a><2>benzazepine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(cyclohexylcarbonyl)-4-thioxo-1,2,3,4,6,7,8,12b-octahydropyrazino<2,1-a><2>benzazepine(121654-79-3)
• EPA Substance Registry System: 2-(cyclohexylcarbonyl)-4-thioxo-1,2,3,4,6,7,8,12b-octahydropyrazino<2,1-a><2>benzazepine(121654-79-3)

Safety Data

• Hazardous Substances Data: 121654-79-3(Hazardous Substances Data)

Upstream product

• 98123-61-6 2H-4-oxo-1,2,3,4,6,7,8,12b-octahydropyrazino<2,1-a><2>benzazepine 
• 98123-74-1 2-(triphenylmethyl)-4-thioxo-1,2,3,4,6,7,8,12b-octahydropyrazino<2,1-a><2>benzazepine 
• 121654-85-1 2-(triphenylmethyl)-4-oxo-1,2,3,4,6,7,8,12b-octahydropyrazino<2,1-a><2>benzazepine 
• 121654-45-3 2-benzyl-4-oxo-1,2,3,4,6,7,8,12b-octahydropyrazino<2,1-a><2>benzazepine 
• 98123-84-3 1-(3-phenylpropyl)-4-benzyl-piperazine-2,6-dione 
• 98123-85-4 1-(3-phenylpropyl)-4-benzyl-2-hydroxy-6-oxopiperazine 
• 2038-57-5 3-Phenylpropan-1-amine 
• 121654-86-2 2H-4-thioxo-1,2,3,4,6,7,8,12b-octahydropyrazino<2,1-a><2>benzazepine 
• 2719-27-9 cyclohexanylcarbonyl chloride 
• 98123-67-2 2-(cyclohexylcarbonyl)-4-oxo-1,2,3,4,6,7,8,12b-octahydropyrazino[2,1-a][2]benzazepine 

Relevant articles and documents

Synthesis and Anthelmintic Activity of a Series of Pyrazinobenzazepine Derivatives

A series of 1,2,3,4,6,7,8,12b-octahydropyrazinobenzazepine derivatives was prepared and the cestocidal activity of the compounds evaluated in an in vitro Taenia crassiceps screen.Many of these derivatives proved to be highly active, and 2-(cyclohexylcarbonyl)-4-oxo-1,2,3,4,6,7,8,12b-octahydropyrazinobenzazepine, epsiprantel (BAN) (22), was selected for further development.The structure-activity relationships are discussed.