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(2-chlorophenyl)iodanediyl diacetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

59696-04-7

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59696-04-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59696-04-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,6,9 and 6 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 59696-04:
(7*5)+(6*9)+(5*6)+(4*9)+(3*6)+(2*0)+(1*4)=177
177 % 10 = 7
So 59696-04-7 is a valid CAS Registry Number.

59696-04-7Relevant academic research and scientific papers

Syntheses of (diacetoxyiodo)arenes or iodylarenes from iodoarenes, with sodium periodate as the oxidant

Kazmierczak, Pawel,Skulski, Lech,Kraszkiewicz, Lukasz

, p. 881 - 891 (2001)

Easy, safe, and effective novel methods for preparing either (diacetoxyiodo)-(arenes, ArI(OAc)2, or iodylarenes, ArIO2, from the corresponding iodoarenes, ArI, using sodium periodate as the oxidant are presented in this paper. In order to obtain 2- and 4-iodylbenzoic acids, the respective sodium salts of 2- and 4-iodobenzoic acids should be used as the starting substrates, because mixtures containing the corresponding iodosyl derivatives as the main products along with the intended iodyl compounds are produced from the free parent acids.

Tandem catalytic C(sp3)-H amination/sila-sonogashira-hagihara coupling reactions with iodine reagents

Buendia, Julien,Darses, Benjamin,Dauban, Philippe

supporting information, p. 5697 - 5701 (2015/06/16)

A new tandem C-N and C-C bond-forming reaction has been achieved through RhII/Pd0 catalysis. The sequence first involves an iodine(III) oxidant, then the in situ generated iodine(I) by-product is used as a coupling partner. The overall process demonstrates the synthetic value of iodoarenes produced in trivalent iodine reagent mediated oxidations. I(003) is a double agent: A tandem C-N and C-C bond-forming reaction has been achieved through RhII/Pd0 catalysis. The sequence first involves an iodine(III) oxidant, then the in situ generated iodine(I) by-product is used as a coupling partner. The overall process affords complex building blocks with high yields, and demonstrates the synthetic value of iodoarenes produced in trivalent iodine reagent mediated oxidations.

Easy preparation of (diacetoxyiodo)arenes from iodoarenes with sodium percarbonate as the oxidant

Zielinska, Agnieszka,Skulski, Lech

, p. 806 - 809 (2007/10/03)

Easy and effective preparations of nearly pure (diacetoxyiodo)arenes, ArI(OAc)2, from iodoarenes, ArI, are reported. In most cases the crude colorless products thus obtained need not be further purified, i.e., by recrystallization. As an example, the PhI(OAc)2 thus prepared was 99% pure (by iodometry).

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