123794-30-9

Basic information

• Product Name: N-{2-[5-(methylsulfanyl)-4-oxo-4H-pyrido[2,3,4-kl]acridin-6-yl]ethyl}acetamide
• Synonyms: acetamide, N-[2-[5-(methylthio)-4-oxo-4H-pyrido[2,3,4-kl]acridin-6-yl]ethyl]-
• CAS NO: 123794-30-9
• Molecular Formula: C₂₀H₁₇N₃O₂S
• Molecular Weight: 363.4329
• Mol File: 123794-30-9.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 706.6°C at 760 mmHg
• Flash Point: 381.1°C
• Density: 1.38g/cm³
• Vapor Pressure: 8.16E-20mmHg at 25°C
• Refractive Index: 1.718
• CAS DataBase Reference: N-{2-[5-(methylsulfanyl)-4-oxo-4H-pyrido[2,3,4-kl]acridin-6-yl]ethyl}acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-{2-[5-(methylsulfanyl)-4-oxo-4H-pyrido[2,3,4-kl]acridin-6-yl]ethyl}acetamide(123794-30-9)
• EPA Substance Registry System: N-{2-[5-(methylsulfanyl)-4-oxo-4H-pyrido[2,3,4-kl]acridin-6-yl]ethyl}acetamide(123794-30-9)

Safety Data

• Hazardous Substances Data: 123794-30-9(Hazardous Substances Data)

Upstream product

• 74-93-1 methylthiol 
• 158734-25-9 cystodytine J 
• 156489-08-6 Acetic acid 2-[2,7-dichloro-5,8-dimethoxy-4-(2-nitro-phenyl)-quinolin-6-yl]-ethyl ester 
• 156489-12-2 N-{2-[2,7-Dichloro-5,8-dimethoxy-4-(2-nitro-phenyl)-quinolin-6-yl]-ethyl}-acetamide 
• 156489-13-3 N-{2-[2,7-Dichloro-4-(2-nitro-phenyl)-5,8-dioxo-5,8-dihydro-quinolin-6-yl]-ethyl}-acetamide 
• 156489-11-1 [2,7-Dichloro-5,8-dimethoxy-4-(2-nitro-phenyl)-quinolin-6-yl]-acetonitrile 
• 1027943-01-6 2-[2,7-Dichloro-5,8-dimethoxy-4-(2-nitro-phenyl)-quinolin-6-yl]-ethylamine 
• 156489-09-7 2-[2,7-Dichloro-5,8-dimethoxy-4-(2-nitro-phenyl)-quinolin-6-yl]-ethanol 
• 156489-10-0 [2,7-Dichloro-5,8-dimethoxy-4-(2-nitro-phenyl)-quinolin-6-yl]-acetaldehyde 
• 156489-14-4 N-{2-[2-Chloro-7-methylsulfanyl-4-(2-nitro-phenyl)-5,8-dioxo-5,8-dihydro-quinolin-6-yl]-ethyl}-acetamide 

Relevant articles and documents

Diplamine, a cytotoxic polyaromatic alkaloid from the tunicate Diplosoma sp.

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Total Synthesis of Cystodytin J, Diplamine and Shermilamine B

Concise, efficient total syntheses of three cytotoxic marine alkaloids are described.Key phases of the synthesis are a useful pyridine-forming reaction and a triplet-sensitized thermophotolysis of an aryl azide that established a C-N bond to an unactivate