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2,3,3-Tris(4-methoxyphenyl)-2-propenal is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

96784-48-4

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96784-48-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96784-48-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,7,8 and 4 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 96784-48:
(7*9)+(6*6)+(5*7)+(4*8)+(3*4)+(2*4)+(1*8)=194
194 % 10 = 4
So 96784-48-4 is a valid CAS Registry Number.

96784-48-4Downstream Products

96784-48-4Relevant academic research and scientific papers

The Facile Synthesis of Dihydrofurans by the Oxidation of Olefins with Tris(2,4-pentanedionato)manganese(III)

Nishino, Hiroshi

, p. 1922 - 1927 (2007/10/02)

Eleven olefins were oxidized with tris(2,4-pentanedionato)manganese(III) at the reflux temperature to give the corresponding 3-acetyl-2-methyl-4,5-dihydrofurans in good yields.The oxidation of 9-benzylidene-9,10-dihydroanthracene under the same reaction conditions did not produce the corresponding dihydrofuran, but 9--9,10-dihydroxyanthracene.When 1,1-diphenylethene was oxidized at room temperature, 3-acetyl-2-hydroperoxy-2-methyl-5,5-diphenyltetrahydrofuran was obtained in a high yield.The effects of the solvent and the additives on the yield of dihydrofuran, the comparable reactivities of other (2,4-pentanedionato)metal complexes, such as Co(III), Cr(III), Fe(III), and Cu(II), and the reaction mechanism are discussed.

Reaction of Olefins with Malonamide in the Presence of Manganese(III) Acetate. Formation of α,β-Unsaturated γ-Lactones and γ-Lactams

Nishino, Hiroshi

, p. 217 - 222 (2007/10/02)

The reaction of olefins with malonamide in the presence of manganese(III) acetate gave 2-buten-4-olides and/or 1H-pyrrol-2(5H)-ones in one-step, short reaction time and moderate yields.The product distribution can be accounted for in terms of the stabilization of the intermediate carbocation in the oxidation process.The synthetic application and limitation, and the oxidation mechanism for the formations of α,β-unsaturated γ-lactones and γ-lactams are discussed.

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