1213776-86-3

Basic information

• Product Name: 3-hydroxy-5,5-dimethyl-2-(2-methyl-1-(2,4,6-trihydroxy-3-(1-(2-hydroxy-4,4-dimethyl-6-oxocyclohex-1-enyl)-2-methylpropyl)-5-isobutyrylphenyl)propyl)cyclohex-2-enone
• Synonyms: 3-hydroxy-5,5-dimethyl-2-(2-methyl-1-(2,4,6-trihydroxy-3-(1-(2-hydroxy-4,4-dimethyl-6-oxocyclohex-1-enyl)-2-methylpropyl)-5-isobutyrylphenyl)propyl)cyclohex-2-enone
• CAS NO: 1213776-86-3
• Molecular Weight: 584.75
• Mol File: 1213776-86-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 3-hydroxy-5,5-dimethyl-2-(2-methyl-1-(2,4,6-trihydroxy-3-(1-(2-hydroxy-4,4-dimethyl-6-oxocyclohex-1-enyl)-2-methylpropyl)-5-isobutyrylphenyl)propyl)cyclohex-2-enone(CAS DataBase Reference)
• NIST Chemistry Reference: 3-hydroxy-5,5-dimethyl-2-(2-methyl-1-(2,4,6-trihydroxy-3-(1-(2-hydroxy-4,4-dimethyl-6-oxocyclohex-1-enyl)-2-methylpropyl)-5-isobutyrylphenyl)propyl)cyclohex-2-enone(1213776-86-3)
• EPA Substance Registry System: 3-hydroxy-5,5-dimethyl-2-(2-methyl-1-(2,4,6-trihydroxy-3-(1-(2-hydroxy-4,4-dimethyl-6-oxocyclohex-1-enyl)-2-methylpropyl)-5-isobutyrylphenyl)propyl)cyclohex-2-enone(1213776-86-3)

Safety Data

• Hazardous Substances Data: 1213776-86-3(Hazardous Substances Data)

Upstream product

• 35458-21-0 phlorisobutyrophenone 
• 126-81-8 dimedone 
• 78-84-2 isobutyraldehyde 
• 3471-13-4 dimedone 
• 108-73-6 3,5-dihydroxyphenol 
• 83814-58-8 5,5-dimethyl-2-(2-methyl)propylidenecyclohexane-1,3-dione 

Relevant articles and documents

Metal catalysed versus organocatalysed stereoselective synthesis: The concrete case of myrtucommulones

Myrtucommulones belong to a class of pharmacologically active natural compounds which offer various alternatives to the treatment of pain, inflammation and cancer. Their stereoselective synthesis remains therefore a key-challenge towards its use in the pharmaceutical industry. In the present work myrtucommulone A and B were synthesised through metal catalysis with 81 and 72% ee respectively. Thanks to the use of cinchonidine as an organocatalyst, 82 and 84% de were reached for myrtucommulone A and myrtucommulone F respectively. Simultaneously, a new synthetic method emerged and gave access to new range of possibilities for the preparation of myrtucommulone derivatives under mild conditions or through a one-pot reaction.