565433-79-6

Basic information

• Product Name: 2-(2,5-Bis-acetylsulfanyl-4-methyl-3,6-dioxo-piperazin-1-yl)-3-methoxy-benzoic acid methyl ester
• CAS NO: 565433-79-6
• Molecular Weight: 440.498
• Mol File: 565433-79-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-(2,5-Bis-acetylsulfanyl-4-methyl-3,6-dioxo-piperazin-1-yl)-3-methoxy-benzoic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2,5-Bis-acetylsulfanyl-4-methyl-3,6-dioxo-piperazin-1-yl)-3-methoxy-benzoic acid methyl ester(565433-79-6)
• EPA Substance Registry System: 2-(2,5-Bis-acetylsulfanyl-4-methyl-3,6-dioxo-piperazin-1-yl)-3-methoxy-benzoic acid methyl ester(565433-79-6)

Safety Data

• Hazardous Substances Data: 565433-79-6(Hazardous Substances Data)

Upstream product

• 5625-52-5 1-methylpiperazin-2,5-dione 
• 50627-32-2 3-methoxy-2-(4-methyl-2,5-dioxo-piperazin-1-yl)-benzoic acid methyl ester 
• 50627-31-1 2-iodo-3-methoxybenzoic acid 
• 10387-40-3 potassium thioacetate 

Downstream Products

• 79247-66-8 C₂₉H₂₈N₂O₅S₂ 
• 79247-66-8 C₂₉H₂₈N₂O₅S₂ 
• 79247-67-9 C₂₁H₂₀N₂O₅S₂ 
• 79247-67-9 C₂₁H₂₀N₂O₅S₂ 
• 49593-04-6 (1R,3S,5R)-6-(2-Chloromethyl-6-methoxy-phenyl)-3-(4-methoxy-phenyl)-8-methyl-2,4-dithia-6,8-diaza-bicyclo[3.2.2]nonane-7,9-dione 
• 49593-04-6 (1R,3R,5R)-6-(2-Chloromethyl-6-methoxy-phenyl)-3-(4-methoxy-phenyl)-8-methyl-2,4-dithia-6,8-diaza-bicyclo[3.2.2]nonane-7,9-dione 
• 79247-65-7 (1S,3R,5S)-1-Benzyloxymethyl-6-(2-chloromethyl-6-methoxy-phenyl)-3-(4-methoxy-phenyl)-8-methyl-2,4-dithia-6,8-diaza-bicyclo[3.2.2]nonane-7,9-dione 
• 50627-34-4 3-methoxy-2-[3ξ-(4-methoxy-phenyl)-8-methyl-7,9-dioxo-2,4-dithia-6,8-diaza-bicyclo[3.2.2]non-6-yl]-benzoic acid methyl ester 
• 79247-64-6 C₂₁H₂₀N₂O₄S₂ 
• 79247-63-5 (1R,5R)-6-(2-Hydroxymethyl-6-methoxy-phenyl)-3-(4-methoxy-phenyl)-8-methyl-2,4-dithia-6,8-diaza-bicyclo[3.2.2]nonane-7,9-dione 
• 1668-07-1 dl-dehydrogliotoxin 

Relevant articles and documents

TOTAL SYNTHESIS OF GLIOTOXIN, DEHYDROGLIOTOXIN AND HYALODENDRIN

Two general methods, Method A and Method B in Scheme 19, to synthesize epidithiapiperazinediones, are described.A total synthesis of racemic and optically active gliotoxin (1) and of racemic dehydrogliotoxin (53) was achieved by using Method A, whereas a total synthesis of racemic hyalodendrin (52) was completed by using Method B.