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1-Propanone, 3-(4-methoxyphenyl)-3-(4-morpholinyl)-1-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

94577-08-9

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94577-08-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 94577-08-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,5,7 and 7 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 94577-08:
(7*9)+(6*4)+(5*5)+(4*7)+(3*7)+(2*0)+(1*8)=169
169 % 10 = 9
So 94577-08-9 is a valid CAS Registry Number.

94577-08-9Relevant academic research and scientific papers

MgO nanoparticles as an efficient and reusable catalyst for aza-Michael reaction

Tajbakhsh, Mahmood,Farhang, Maryam,Hosseini, Ali Asghar

, p. 665 - 672 (2014)

MgO nanoparticles were prepared by an improved sol-gel technique which appeared to have narrow size distributions. The synthesized magnesium oxide nanoparticles were used as an efficient catalyst in aza-Michael reaction for addition of amines to a series of α,β-unsaturated carbonyl compounds and nitro olefins under solvent-free conditions at room temperature to afford high yields of the β-amino carbonyl and β-nitro amines. The catalyst can be recovered and reused at least five successive runs without loss of activity. Graphical abstract: [Figure not available: see fulltext.]

Stereoselective photocyclization to 2-aminocyclopropanols by photolysis of β-aminoketones and oxidative ring opening to enaminones

Weigel, Wilfried,Schiller, Sabine,Henning, Hans-Georg

, p. 7855 - 7866 (2007/10/03)

Irradiation of β-aminopropiophenones 1 leads to the formation of 2-aminocyclopropanols 2 which can undergo oxidative ring opening to give enaminones 3. The regioselectivity of cyclopropanol formation of the α-benzyl substituted 1 is determined by the preferred charge transfer interaction between the photoexcited benzoyl chromophore and the amino group. The photocyclizations of the α- or β-substituted 1 proceed stereoselectively. No photoracemization of the pure enantiomers of 1m, independent of the solvent polarity was observed. Aryl or alkyl substituents at the C(3)- or C(2)-ring atom stabilize the cyclopropanol derivatives. The formation of 3 indicates regioselective C(1)-C(2) ring opening of 2 probably by localization of the excitation energy.

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