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1-bromo-4-iodosylbenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

69180-63-8

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69180-63-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69180-63-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,1,8 and 0 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 69180-63:
(7*6)+(6*9)+(5*1)+(4*8)+(3*0)+(2*6)+(1*3)=148
148 % 10 = 8
So 69180-63-8 is a valid CAS Registry Number.

69180-63-8Upstream product

69180-63-8Relevant academic research and scientific papers

Synthesis of Diverse Aryliodine(III) Reagents by Anodic Oxidation?

Zu, Bing,Ke, Jie,Guo, Yonghong,He, Chuan

, p. 627 - 632 (2021)

An anodic oxidation enabled synthesis of hypervalent iodine(III) reagents from aryl iodides is demonstrated. Under mild electrochemical conditions, a range of aryliodine(III) reagents including iodosylarenes, (difunctionaliodo)arenes, benziodoxoles and diaryliodonium salts can be efficiently synthesized and derivatized in good to excellent yields with high selectivity. As only electrons serve as the oxidation reagents, this method offers a more straightforward and sustainable manner avoiding the use of expensive or hazardous chemical oxidants.

Metal-Free O-Arylation of Carboxylic Acid by Active Diaryliodonium(III) Intermediates Generated in situ from Iodosoarenes

Dohi, Toshifumi,Koseki, Daichi,Sumida, Kohei,Okada, Kana,Mizuno, Serina,Kato, Asami,Morimoto, Koji,Kita, Yasuyuki

, p. 3503 - 3508 (2017/09/13)

The metal-free arylative coupling of carboxylic acids using iodosoarenes without the use of a catalyst and base, which is applicable to even a highly-polar molecule bearing multiple alcohol groups, is reported. The in situ preparation of the reactive diaryliodonium(III) carboxylates is the important key to this approach, and the introduction of the trimethoxybenzene auxiliary enables both the smooth salt formations and the selective aryl transfer events during the couplings. (Figure presented.).

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