220968-18-3

Basic information

• Product Name: 3-dimethylamino-5-(2,6,6-trimethyl-2-cyclohexen-1-yl)-2,4-pentadienal
• Synonyms: 3-dimethylamino-5-(2,6,6-trimethyl-2-cyclohexen-1-yl)-2,4-pentadienal
• CAS NO: 220968-18-3
• Molecular Weight: 247.381
• Mol File: 220968-18-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 3-dimethylamino-5-(2,6,6-trimethyl-2-cyclohexen-1-yl)-2,4-pentadienal(CAS DataBase Reference)
• NIST Chemistry Reference: 3-dimethylamino-5-(2,6,6-trimethyl-2-cyclohexen-1-yl)-2,4-pentadienal(220968-18-3)
• EPA Substance Registry System: 3-dimethylamino-5-(2,6,6-trimethyl-2-cyclohexen-1-yl)-2,4-pentadienal(220968-18-3)

Safety Data

• Hazardous Substances Data: 220968-18-3(Hazardous Substances Data)

Upstream product

• 127-41-3 alpha-ionone 
• 68-12-2 N,N-dimethyl-formamide 

Downstream Products

• 1208251-53-9 ethyl 4-{5-[2-(2,6,6-trimethylcyclohex-2-en-1-yl)ethenyl]-1H-pyrazol-1-yl}benzoate 
• 1208251-77-7 ethyl 4-{3-[2-(2,6,6-trimethylcyclohex-2-en-1-yl)ethenyl]-1H-pyrazol-1-yl}benzoate 
• 1208251-57-3 2-{5-[2-(2,6,6-trimethylcyclohex-2-en-1-yl)ethenyl]-1H-pyrazol-1-yl}pyridine 
• 1208251-80-2 2-{3-[2-(2,6,6-trimethylcyclohex-2-en-1-yl)ethenyl]-1H-pyrazol-1-yl}pyridine 
• 1208251-63-1 4-{5-[2-(2,6,6-trimethylcyclohex-2-en-1-yl)ethenyl]-1H-pyrazol-1-yl}benzenesulfonamide 
• 1208251-65-3 ethyl 2-{5-[2-(2,6,6-trimethylcyclohex-2-en-1-yl)ethenyl]-1H-pyrazol-1-yl}ethanoate 
• 1208251-84-6 ethyl 2-{3-(2-(2,6,6-trimethylcyclohex-2-en-1-yl)ethenyl)-1H-pyrazol-1-yl}ethanoate 
• 1208251-51-7 4-{5-[2-(2,6,6-trimethylcyclohex-2-en-1-yl)ethenyl]-1H-pyrazol-1-yl}benzoic acid 
• 1208251-71-1 1-(2-chlorophenyl)-3-[2-(2,6,6-trimethylcyclohex-2-en-1-yl)ethenyl]-1H-pyrazole 
• 1208251-73-3 1-(4-chlorophenyl)-3-[2-(2,6,6-trimethylcyclohex-2-en-1-yl)ethenyl]-1H-pyrazole 
• 1208251-69-7 1-phenyl-3-[2-(2,6,6-trimethylcyclohex-2-en-1-yl)ethenyl]-1H-pyrazol 
• 1208251-75-5 1-(4-bromophenyl)-3-[2-(2,6,6-trimethylcyclohex-2-en-1-yl)ethenyl]-1H-pyrazole 

Relevant articles and documents

Synthesis and biological evaluation of novel heterocyclic ionone-like derivatives as anti-inflammatory agents

Five- and six-membered heterocyclic ionone-like derivatives 4-6 have been synthesised in one step and with good yield from the key intermediate 3a and appropriate bifunctional reagents. Four were active as inhibitors of the respiratory burst of human neut