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tetramethylammonium 4-(dimethylamino)benzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

70697-58-4

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70697-58-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70697-58-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,6,9 and 7 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 70697-58:
(7*7)+(6*0)+(5*6)+(4*9)+(3*7)+(2*5)+(1*8)=154
154 % 10 = 4
So 70697-58-4 is a valid CAS Registry Number.

70697-58-4Relevant academic research and scientific papers

Benzoate Cyclometalation Enables Oxidative Addition of Haloarenes at a Ru(II) Center

Simonetti, Marco,Kuniyil, Rositha,Macgregor, Stuart A.,Larrosa, Igor

supporting information, p. 11836 - 11847 (2018/09/29)

The first Ru(II)-catalyzed arylation of substrates without a directing group was recently developed. Remarkably, this process only worked in the presence of a benzoate additive, found to be crucial for the oxidative addition step at Ru(II). However, the exact mode of action of the benzoate was unknown. Herein, we disclose a mechanistic study that elucidates the key role of the benzoate salt in the C-H arylation of fluoroarenes with aryl halides. Through a combination of rationally designed stoichiometric experiments and DFT studies, we demonstrate that the aryl-Ru(II) species arising from initial C-H activation of the fluoroarene undergoes cyclometalation with the benzoate to generate an anionic Ru(II) intermediate. The enhanced lability of this intermediate, coupled with the electron-rich anionic Ru(II) metal center renders the oxidative addition of the aryl halide accessible. The role of an additional (NMe4)OC(CF3)3 additive in facilitating the overall arylation process is also shown to be linked to a shift in the C-H pre-equilibrium associated with benzoate cyclometalation.

SYNTHESIS OF ACETAL COMPOUNDS USING ZWITTERIONIC CATALYSTS

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Paragraph 0109, (2015/05/19)

A process for the preparation of optionally asymmetric acetal compounds, comprising reacting a compound containing a hydroxyl group with a vinylether compound in the presence of a zwitterionic catalyst including at least one basic nitrogen containing structural fragment and at least one sulfonic acid group in its structure, with the proviso that the basic nitrogen on sulfonic acid molar ratio is 1 over 1.

Tertiary aromatic amine accelerators in acrylic resin

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, (2008/06/13)

Tertiary aromatic amines derived from aminoglutethimide or para-aminophenylacetic acid act as accelerators for the peroxide catalyzed polymerization of acrylic resins, especially methacrylates, acrylates and unsaturated polyesters. The amines are characte

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