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difluoro(4-methoxyphenyl)-λ3-iodane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

58636-76-3

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58636-76-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58636-76-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,6,3 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 58636-76:
(7*5)+(6*8)+(5*6)+(4*3)+(3*6)+(2*7)+(1*6)=163
163 % 10 = 3
So 58636-76-3 is a valid CAS Registry Number.

58636-76-3Relevant academic research and scientific papers

Electrolytic Partial Fluorination of Organic Compounds. 14. The First Electrosynthesis of Hypervalent Iodobenzene Difluoride Derivatives and Its Application to Indirect Anodic gem-Difluorination

Fuchigami, Toshio,Fujita, Toshiyasu

, p. 7190 - 7192 (1994)

The electrosynthesis of hypervalent iodobenzene difluorides was accomplished by anodic oxidation of p-nitro- and p-methoxyiodobenzenes with Et3N*3HF in anhydrous acetonitrile, and p-methoxyiodobenzene difluoride was used as a mediator for indirect anodic

Fluorocyclization of N-Propargyl Carboxamides by λ3-Iodane Catalysts with Coordinating Substituents

Takahashi, Shunsuke,Umakoshi, Yuki,Nakayama, Kaii,Okada, Yohei,Zhdankin, Viktor V.,Yoshimura, Akira,Saito, Akio

supporting information, p. 2997 - 3003 (2020/06/17)

Aiming at the enhanced catalytic activity of fluoro-λ3-iodane generated from iodoarene precatalyst with Selectfluor and HF?pyridine, this study focused on the λ3-iodanes bearing coordinating substituents. Compared to 4-iodoanisole as a precatalyst of our previous method, N-methyl-2-iodobenzamide or 2-iodobenzamide worked well in the fluorocyclization of N-propargyl carboxamides to oxazoles. Control experiments suggest the equilibrium mixture of iodane-amine complexes and cyclic iodane fluorides would be involved in the present catalysis. (Figure presented.).

Deconstructing the Catalytic, Vicinal Difluorination of Alkenes: HF-Free Synthesis and Structural Study of p-TolIF2

Sarie, Jér?me C.,Thiehoff, Christian,Mudd, Richard J.,Daniliuc, Constantin G.,Kehr, Gerald,Gilmour, Ryan

, p. 11792 - 11798 (2017/11/24)

Recently, contemporaneous strategies to achieve the vicinal difluorination of alkenes via an I(I)/I(III) catalysis manifold were independently reported by this laboratory and by Jacobsen and co-workers. Both strategies proceed through a transient ArI(III)

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