145674-58-4

Basic information

• Product Name: 2-isopropyl-4,4-dimethoxy-5-methyl-cyclohexa-2,5-dienone
• Synonyms: 2-isopropyl-4,4-dimethoxy-5-methyl-cyclohexa-2,5-dienone
• CAS NO: 145674-58-4
• Molecular Weight: 210.273
• Mol File: 145674-58-4.mol

Chemical Properties

• CAS DataBase Reference: 2-isopropyl-4,4-dimethoxy-5-methyl-cyclohexa-2,5-dienone(CAS DataBase Reference)
• NIST Chemistry Reference: 2-isopropyl-4,4-dimethoxy-5-methyl-cyclohexa-2,5-dienone(145674-58-4)
• EPA Substance Registry System: 2-isopropyl-4,4-dimethoxy-5-methyl-cyclohexa-2,5-dienone(145674-58-4)

Safety Data

• Hazardous Substances Data: 145674-58-4(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 99-87-6 4-methylisopropylbenzene 
• 89-83-8 thymol 
• 124-41-4 sodium methylate 

Downstream Products

• 490-91-5 thymoquinone 

Relevant articles and documents

Electrochemical Methoxylation of Thymol and Carvacrol

Anodic oxidation of methanolic solutions of thymol and carvacrol, each in a single cell at constant current intensity, afforded substitution and addition products in the former case and only a nucleophilic-addition product in the latter.

Anodic Oxidation of Isopropyl and Tert-Butylbenzenes. Synthetic Routes to Certain Cyclohexa-1,4-Dienes

The anodic methoxylation of p-cymene and p-tert-butyltoluene afforded side-chain methoxylated products as well as nuclear-addition products.For nuclear-addition products both cis/trans isomers are possible and in both cases the cis isomer is in higher proportion than the trans one.The anodic methoxylation of 1,4-di-tert-butylbenzene afforded only nuclear-addition products and the anodic methoxylation of 1,4-di-isopropylbenzene afforded only side-chain products.A probable mechanism is provided.