893408-51-0

Basic information

• Product Name: 3-acetyl-1,4-dihydroxy-5-(4-benzyloxy-3,5-diisopropylphenyl)-2(1H)-pyridone
• Synonyms: 3-acetyl-1,4-dihydroxy-5-(4-benzyloxy-3,5-diisopropylphenyl)-2(1H)-pyridone
• CAS NO: 893408-51-0
• Molecular Weight: 435.52
• Mol File: 893408-51-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3-acetyl-1,4-dihydroxy-5-(4-benzyloxy-3,5-diisopropylphenyl)-2(1H)-pyridone(CAS DataBase Reference)
• NIST Chemistry Reference: 3-acetyl-1,4-dihydroxy-5-(4-benzyloxy-3,5-diisopropylphenyl)-2(1H)-pyridone(893408-51-0)
• EPA Substance Registry System: 3-acetyl-1,4-dihydroxy-5-(4-benzyloxy-3,5-diisopropylphenyl)-2(1H)-pyridone(893408-51-0)

Safety Data

• Hazardous Substances Data: 893408-51-0(Hazardous Substances Data)

Upstream product

• 561068-86-8 3-acetyl-N-benzyloxy-5-bromo-4-hydroxy-2(1H)-pyridone 
• 561068-89-1 3-(N-benzyloxy-N-(3-oxobutyryl)amino)propanoic acid 
• 561068-88-0 methyl 3-(N-benzyloxy-N-(3-oxobutyryl)amino)propanoate 
• 561068-90-4 3-acetyl-N-benzyloxy-5,6-dihydro-4-hydroxy-2(1H)-pyridone 
• 561068-91-5 3-acetyl-N-benzyloxy-4-hydroxy-2(1H)-pyridone 
• 2432-03-3 4-bromopropofol 
• 2078-54-8 2,6-diisopropylphenol 
• 893408-45-2 4-benzyloxy-3,5-diisopropylphenylboronic acid 
• 893408-44-1 2-(benzyloxy)-5-bromo-1,3-diisopropylbenzene 
• 893408-46-3 3-acetyl-N-benzyloxy-5-(4-benzyloxy-3,5-diisopropylphenyl)-4-hydroxy-2(1H)-pyridone 

Downstream Products

• 893408-47-4 3-acetyl-1,4-dihydroxy-5-(3,5-diisopropyl-4-hydroxyphenyl)-2(1H)-pyridone 

Relevant articles and documents

Studies towards the biomimetic synthesis of pyridomacrolidin

A possible biomimetic synthesis of pyridomacrolidin has been proposed and experimentally supported by carrying out a model study. Regio and stereospecific [3+2] cycloaddition of an in situ generated unusual di-tert-butylated acyl nitrone with Z-2-cyclodecenone and subsequent aromatisation was the key step in our proposed biomimetic synthesis. Finally a pyridomacrolidin analogue was prepared via Friedel-Crafts di-de-t-butylation of the cycloadduct.