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2-Benzoyl-1-(morpholin-4-yl)-1-cyclohexene is a complex organic compound with the molecular formula C16H19NO2. It features a cyclohexene ring, which is a six-carbon ring with one double bond, and a benzoyl group (C6H5-CO) attached to the second carbon. Additionally, a morpholin-4-yl group is connected to the first carbon of the cyclohexene ring. 2-benzoyl-1-(morpholin-4-yl)-1-cyclohexene is known for its potential applications in the synthesis of pharmaceuticals and other organic compounds due to its unique structure and reactivity. It is an example of a functionalized cyclohexene derivative, which can be further modified or used as a building block in the creation of more complex molecules.

5292-56-8

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5292-56-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5292-56-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,9 and 2 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5292-56:
(6*5)+(5*2)+(4*9)+(3*2)+(2*5)+(1*6)=98
98 % 10 = 8
So 5292-56-8 is a valid CAS Registry Number.

5292-56-8Relevant academic research and scientific papers

One-Pot Synthesis of 3-Oxocycloalka[c]pyridines

Geronikaki, A.,Hakobyan, E. K.,Hovakimyan, A. A.,Kartsev, V. G.,Sirakanyan, S. N.

, p. 1748 - 1752 (2021/12/13)

Abstract: A new efficient one-pot procedure has been developed for the synthesis of 1-substituted partially hydrogenated 3-oxocycloalka[c]pyridine-4-carbonitriles by reaction of cyclopentanone or cyclohexanone with morpholine, acyl chloride, and cyanoacetamide. The proposed procedure is advantageous due to shorter reaction time and smaller amounts of the solvents and reactants.

Synthesis and characterization of new long-wavelength-absorbing oxonol dyes from the 2,2-difluoro-1,3,2-dioxaborine type

Halik, Marcus,Hartmann, Horst

, p. 2511 - 2517 (2007/10/03)

By starting from methyl- and methylene-substituted 2,2-difluoro-1,3,2-dioxaborines 5, 20, and 21 and different types of reactive formyl derivatives (14-17) a series of anionic, cationic, and betainic methine dyes has been prepared. These dioxaborine dyes

FUNCTIONALIZED CHLOROENAMINES IN AMINOCYCLOPROPANE SYNTHESIS - V. SYNTHESIS AND REACTIONS OF AMINOCYCLOPROPYLKETONES

Vilsmaier, Elmar,Doerrenbaecher, Ralph,Mueller, Lutz

, p. 8103 - 8116 (2007/10/02)

Conjugated acylated chloroenamines 5A,C were available by chlorination of mixtures of acylated enamines 8A,C/9A,C by NCS at 0 deg C.Nonconjugated chloroenamines 10Aa and 10Ba could be obtained by NCS-chlorination of the conjugated acylenamines 9A,B at low temperature.Reaction of 5Aa-5Ac, 5Ae, 5Af with cyanide produced morpholinocyclopropylketones 11A.In two cases aminofurans 12Ad and 12Ca resulted as products of this reaction.More generally amino-aryl-furans 12 were formed by thermolysis of the aryl-cyclopropylketones 11.Amino-alkyl-furans as 12Ae and 12Af only could be trapped by a Diels-Alder reaction leading to 16Ae and 16Af.Epoxyenamines 29A,B unexpectedly were produced from the interaction of cyanide with the chloroenamines 10Aa and 10Ba.

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