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(E)-3,7-dimethylocta-2,6-dien-1-yl 3,5-dinitrobenzoate is a complex organic compound with the molecular formula C17H19NO4. It is characterized by a conjugated diene system with two double bonds in the 2,6-positions, and two methyl groups at the 3 and 7 positions. The molecule is esterified with 3,5-dinitrobenzoic acid, which provides it with two nitro groups at the 3 and 5 positions of the benzene ring. (E)-3,7-dimethylocta-2,6-dien-1-yl 3,5-dinitrobenzoate is known for its potential applications in the synthesis of various organic compounds and as a chemical intermediate in the pharmaceutical and chemical industries. Its structure and properties make it a versatile building block for the creation of more complex molecules, particularly in the area of natural product synthesis and the development of new drugs.

7070-10-2

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7070-10-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7070-10-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,7 and 0 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7070-10:
(6*7)+(5*0)+(4*7)+(3*0)+(2*1)+(1*0)=72
72 % 10 = 2
So 7070-10-2 is a valid CAS Registry Number.

7070-10-2Downstream Products

7070-10-2Relevant academic research and scientific papers

Dirhodium(II)-Mediated Alkene Epoxidation with Iodine(III) Oxidants

Nasrallah, Ali,Grelier, Gwendal,Lapuh, Maria Ivana,Duran, Fernando J.,Darses, Benjamin,Dauban, Philippe

supporting information, p. 5836 - 5842 (2018/11/24)

Dirhodium(II) complexes and iodine(III) oxidants have found useful applications in synthetic nitrene chemistry. In this study, the combination of the dirhodium(II) complex Rh2(tpa)4 (tpa = triphenylacetate) with the iodine(III) oxidant PhI(OPiv)2 is shown to promote the epoxidation of alkenes in the presence of 2 equivalents of water. The reaction can be applied to diversely substituted alkenes and the corresponding epoxides are isolated with yields of up to 90 %. A possible mechanism involves the dirhodium(II) complex as a Lewis acid species that would tune the oxidizing character of the iodine(III) reagent.

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