24706-48-7

Basic information

• Product Name: 2-cyclohexen-1-one, 3-[(4-methoxyphenyl)amino]-5,5-dimethy
• Synonyms: 2-cyclohexen-1-one, 3-[(4-methoxyphenyl)amino]-5,5-dimethy;3-[(4-methoxyphenyl)amino]-5,5-dimethylcyclohex-2-en-1-one;3-[(4-methoxyphenyl)amino]-5,5-dimethyl-1-cyclohex-2-enone
• CAS NO: 24706-48-7
• Molecular Formula: C₁₅H₁₉NO₂
• Molecular Weight: 245.31686
• Mol File: 24706-48-7.mol
• Article Data: 32

Chemical Properties

• Melting Point: 186-188 °C
• Boiling Point: 370.1±42.0 °C(Predicted)
• Appearance: /
• Density: 1.107±0.06 g/cm3(Predicted)
• PKA: 1.26±0.40(Predicted)
• CAS DataBase Reference: 2-cyclohexen-1-one, 3-[(4-methoxyphenyl)amino]-5,5-dimethy(CAS DataBase Reference)
• NIST Chemistry Reference: 2-cyclohexen-1-one, 3-[(4-methoxyphenyl)amino]-5,5-dimethy(24706-48-7)
• EPA Substance Registry System: 2-cyclohexen-1-one, 3-[(4-methoxyphenyl)amino]-5,5-dimethy(24706-48-7)

Safety Data

• Hazardous Substances Data: 24706-48-7(Hazardous Substances Data)

Upstream product

• 126-81-8 dimedone 
• 104-94-9 4-methoxy-aniline 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 873-95-0 1-amino-5,5-dimethylcyclohexen-3-one 
• 1001588-86-8 7,7-dimethyl-4-phenyl-4,6,7,8-tetrahydro-2H-1,3-benzoxazine-2,5(3H)-dione 
• 4683-45-8 3-methoxy-5,5-dimethyl-cyclohex-2-enone 

Downstream Products

• 1009033-56-0 5-(4-chlorophenyl)-7,8-dihydro-7,7-dimethyl-10-(4-methoxyphenyl)-5H-indeno[1,2-b]quinolin-9,11(6H,10H)-dione 
• 1180846-53-0 1'-(4-methoxyphenyl)-6',6'-dimethyl-6',7'-dihydro-3H-spiro[furan-2,3'-indole]-2',4,4',5(1'H,5'H)-tetraone 
• 1180846-49-4 1'-(4-methoxyphenyl)-6',6'-dimethyl-3-[(Z)-phenyl(phenylamino)methylidene]-6',7'-dihydro-3H-spiro[furan-2,3'-indole]-2',4,4',5(1'H,5'H)-tetraone 
• 1417794-71-8 1-(4-methoxyphenyl)-7,7-dimethyl-4-(2-nitrophenyl)-3,4,7,8-tetrahydroquinoline-2,5(1H,6H)-dione 
• 1591873-45-8 C₃₅H₃₁N₃O₄ 
• 1591873-50-5 C₃₆H₃₃N₃O₄ 
• 1591873-22-1 C₃₅H₃₀N₂O₅ 
• 1591873-33-4 12-(4-hydroxy-5-methyl-2-oxo-2H-pyran-3-yl)-5-(4-methoxyphenyl)-3,3,9-trimethyl-3,4,5,12-tetrahydrodibenzo[b,g][1,8]naphthyridin-1(2H)-one 
• 1591873-27-6 C₃₆H₃₂N₂O₅ 
• 1591873-20-9 2-(4-hydroxy-2-oxo-2H-chromen-3-yl)-5-(4-methoxyphenyl)-3,3-dimethyl-3,4,5,12-tetrahydrodibenzo[b,g][1,8]naphthyridin-1(2H)-one 

Relevant articles and documents

Synthesis of 1,8-Dioxo-decahydroacridine Derivatives via Ru-Catalyzed Acceptorless Dehydrogenative Multicomponent Reaction

A Ru-catalyzed acceptorless dehydrogenative multicomponent reaction has been developed. This reaction offers a cost-effective and simple operational strategy to synthesize biologically active 1,8-dioxodecahydroacridine derivatives. The protocol provides a wide range of substrate scope and various functional groups are also well tolerated under the reaction condition. To shed light on the mechanistic and kinetic study, some controlled experiments and deuterium labeling experiments were executed. A time-dependent product distribution experiment is also presented and the reaction scale-up is performed to highlight the practical utility of this strategy.

Metal-free syntheses of new azocinesviaaddition reactions of enaminones with acenaphthoquinone followed by oxidative cleavages of the corresponding vicinal diols

A one-pot, clean and green procedure is described for the syntheses of new azocine derivativesviaaddition reactions of enaminones with acenaphthoquinone followed by periodic acid-mediated oxidative cleavages of the corresponding vicinal diols. Various derivatives of azocine were prepared and well characterized. The excellent yields, simple synthesis procedure, lack of a need to carry out any tedious work-up and column chromatography, metal-free catalysis, and mild reaction conditions are important features of this protocol.

β-Enaminones over recyclable nano-CoFe2O4: a highly efficient solvent-free green protocol

Abstract: β-Enaminone and its derivatives have emerged among the finest bioactive intermediates. High yields of several β-enaminones (86–97%) are achieved through treatment of substituted aromatic and aliphatic amines with cyclic/acyclic 1,3-diketones, over the magnetically separable cobalt ferrite nanoparticles (CoFe2O4 NPs). The latter was prepared upon co-precipitation. Its purity, fine crystallinity, elemental distributions, morphology, magnetic features, and thermal stability were confirmed by Fourier transform infrared, X-ray diffraction, energy dispersive X-ray spectrometry, scanning electron microscopy, vibrating sample magnetometry, and thermal gravimetric analysis analyses. Thus, CoFe2O4 NPs acted as an excellent green heterogeneous nanocatalyst for synthesis of β-enaminones and gave good recyclability, while showing insignificant loss of their activity. Graphical Abstract: [Figure not available: see fulltext.].