7560-94-3

Basic information

• Product Name: 2-Cyclohexen-1-one, 2,2'-[(4-methoxyphenyl)methylene]bis[3-hydroxy-5,5-dimethyl-
• CAS NO: 7560-94-3
• Molecular Formula: C24H30O5
• Molecular Weight: 398.499
• Mol File: 7560-94-3.mol
• Article Data: 50

Chemical Properties

• CAS DataBase Reference: 2-Cyclohexen-1-one, 2,2'-[(4-methoxyphenyl)methylene]bis[3-hydroxy-5,5-dimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Cyclohexen-1-one, 2,2'-[(4-methoxyphenyl)methylene]bis[3-hydroxy-5,5-dimethyl-(7560-94-3)
• EPA Substance Registry System: 2-Cyclohexen-1-one, 2,2'-[(4-methoxyphenyl)methylene]bis[3-hydroxy-5,5-dimethyl-(7560-94-3)

Safety Data

• Hazardous Substances Data: 7560-94-3(Hazardous Substances Data)

Upstream product

• 123-11-5 4-methoxy-benzaldehyde 
• 126-81-8 dimedone 
• 203731-09-3 4-methoxybenzylidenemethylamine N-oxide 
• 3246-78-4 N-(4-methoxybenzylidene)-4-methylaniline 

Downstream Products

• 181480-21-7 ethyl 4-(4-methoxyphenyl)-2,7,7-trimethyl-5-oxo-1,4,5,6,7,8-hexahydroquinoline-3-carboxylate 
• 1448188-77-9 2,2',2'',2'''-(1,2-bis(4-methoxyphenyl)ethane-1,1,2,2-tetrayl)tetrakis(3-hydroxy-5,5-dimethylcyclohex-2-enone) 
• 118966-43-1 2-(4-methoxyphenyl)-4',4',6,6-tetramethyl-6,7-dihydro-2H-spiro[benzofuran-3,1'-cyclohexane]-2',4,6'(5H)-trione 
• 85972-04-9 N-p'-methoxybenzylidene-o-phenylenediamine 
• 19419-25-1 9-(4-methoxyphenyl)-3,3,6,6-tetramethyl-2,3,4,5,6,7,8,9-octahydro-1H-xanthene-1,8-dione 
• 139484-10-9 2-((4-chlorophenyl)(2-hydroxy-4,4-dimethyl-6-oxocyclohex-1-enyl)methyl)-3-hydroxy-5,5-dimethylcyclohex-2-enone 
• 868273-24-9 2-[(3-chlorophenyl)(2-hydroxy-4,4-dimethyl-6-oxocyclohex-1-en-1-yl)methyl]-3-hydroxy-5,5-dimethylcyclohex-2-en-1-one 
• 156176-94-2 3,3,6,6-tetramethyl-9-(3-nitrophenyl)-1,2,3,4,5,6,7,8,9,10-decahydroacridine-1,8-dione 
• 40588-51-0 9-(4-methylphenyl)-3,3,6,6-tetramethyl-1,2,3,4,5,6,7,8-octahydroxanthene-1,8-dione 
• 37797-12-9 9-(4-hydroxyphenyl)-3,3,6,6-tetramethyl-3,4,5,6,7,9-hexahydro-1H-xanthene-1,8(2H)-dione 
• 30038-64-3 3,3,6,6-tetramethyl-9-(2-nitrophenyl)-2,3,4,5,6,7,8,9-octahydro-1H-xanthene-1,8-dione 
• 7560-71-6 2,2'-(4-nitrophenylmethylene)bis(3-hydroxy-5,5-dimethyl-2-cyclohexene-1-one) 
• 40588-46-3 9-(4-nitrophenyl)-3,3,6,6-tetramethyl-1,2,3,4,5,6,7,8-octahydroxanthene-1,8-dione 
• 40588-50-9 3,3,6,6-tetramethyl-9-(3-nitrophenyl)-3,4,5,6,7,9-hexahydro-1H-xanthene-1,8(2H)-dione 

Relevant articles and documents

2,2′-(Arylmethylene)bis(3-hydroxy-5,5-dimethylcyclohex-2-enone) crystals formation via atom economy reaction and their antioxidant activity

Tetraketones with their diversified biological potencies became a highly significant class of oxygen-containing organic compounds. These are prepared by applying a simple Knoevenagel-Michael cascade procedure with 1,3-dicarbonyl compound and aldehydes. In

Preparation and study of the catalytic application in the synthesis of xanthenedione pharmaceuticals of a hybrid nano-system based on copper, zinc and iron nanoparticles

A novel efficiently mixed transition metal oxides catalytic system with high catalytic activity and heterogeneity constructed of copper and zinc oxide nanoparticles is presented. For preparation of this hybrid catalytic system, carrageenan as a natural polymeric matrix has been chosen to add biocompatibility to the heterogeneous catalyst. Then, the carrageenan textures have been magnetized through the composition with iron oxide nanoparticles. Copper and zinc metallic sites are employed as the main catalytic sites for catalyzing the synthesis of xanthenedione pharmaceutical derivatives from aldehyde and dimedone. Due to the magnetic behavior of the catalyst, the purification process is carried out with high convenience. Herein, a plausible mechanism for the catalytic process is suggested and reusability of the presented catalyst is also investigated. In this report, it has been well-proven that high reaction yields are obtained for xanthenedione derivatives under mild conditions, through applying the presented hybrid catalytic system.

Green synthesis of tetraketones: crystal structure, DFT studies and Hirshfeld surface analysis of 2,2′-((3,4-dimethoxyphenyl) methylene) bis(3-hydroxy-5,5-dimethylcyclohex2-enone)

The present work deals with a practically efficient protocol designed for the synthesis of tetraketones using ultrasound in the presence of boric acid as the catalyst. One of the tetraketone, (3a) was confirmed by crystallographic studies. The molecules i