83814-62-4

Basic information

• Product Name: 7,8-DIHYDRO-2,4-DIISOPROPYL-7,7-DIMETHYL-4H-BENZO[D][1,3]DIOXIN-5(6H)-ONE
• Synonyms: 7,8-DIHYDRO-2,4-DIISOPROPYL-7,7-DIMETHYL-4H-BENZO[D][1,3]DIOXIN-5(6H)-ONE
• CAS NO: 83814-62-4
• Molecular Formula: C₁₆H₂₆O₃
• Molecular Weight: 0
• Mol File: 83814-62-4.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 7,8-DIHYDRO-2,4-DIISOPROPYL-7,7-DIMETHYL-4H-BENZO[D][1,3]DIOXIN-5(6H)-ONE(CAS DataBase Reference)
• NIST Chemistry Reference: 7,8-DIHYDRO-2,4-DIISOPROPYL-7,7-DIMETHYL-4H-BENZO[D][1,3]DIOXIN-5(6H)-ONE(83814-62-4)
• EPA Substance Registry System: 7,8-DIHYDRO-2,4-DIISOPROPYL-7,7-DIMETHYL-4H-BENZO[D][1,3]DIOXIN-5(6H)-ONE(83814-62-4)

Safety Data

• Hazardous Substances Data: 83814-62-4(Hazardous Substances Data)

Upstream product

• 83814-58-8 5,5-dimethyl-2-(2-methyl)propylidenecyclohexane-1,3-dione 
• 78-84-2 isobutyraldehyde 
• 83814-45-3 3-hydroxy-5,5-dimethyl-2-(2-methyl-1-piperidino)propylcyclohex-2-en-1-one 
• 126-81-8 dimedone 

Relevant articles and documents

Plant Growth Regulators in Eucalyptus grandis. V Synthesis of the G-Regulators

Problems associated with earlier synthetic approaches to the G-regulators have been overcome by the use of the Mannich reaction in aprotic media.Under these conditions the Mannich base formed from the reaction of 1,3-diketones and aldehydes is stabilized by internal hydrogen bonding and can be isolated in high yield.In aqueous acid rapid elimination occurs to give the 2-methylene 1,3-diketones, which first enolize then add oxygen to generate the G-regulator structure.The steric limitations of the reactions are examined.