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2-(hydroxymethyl)-4,6-diiodophenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13862-13-0

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13862-13-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13862-13-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,8,6 and 2 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 13862-13:
(7*1)+(6*3)+(5*8)+(4*6)+(3*2)+(2*1)+(1*3)=100
100 % 10 = 0
So 13862-13-0 is a valid CAS Registry Number.

13862-13-0Downstream Products

13862-13-0Relevant academic research and scientific papers

COMPOUND, (CO)POLYMER, COMPOSITION AND METHOD FOR FORMING PATTERN

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Paragraph 0132, (2021/04/10)

The object of the present invention is to provide a composition capable of forming a film with high resolution and high sensitivity. The aforementioned object can be achieved by the halogen-containing polymeric compound represented by the general formula

Lewis Base Catalyzed Intramolecular Reduction of Salicylaldehydes by Pinacol-Derived Chlorohydrosilane

Assoah, Benedicta,Vale, Jo?o R.,Kalenius, Elina,Veiros, Luis F.,Candeias, Nuno R.

supporting information, p. 2910 - 2917 (2018/06/27)

A newly developed stable chlorohydrosilane derived from pinacol is herein described. This was successfully used in the reduction of salicylaldehydes in reasonable to excellent yields (51–97 %). The ability of the hydrosilane to react as a reducing agent is increased upon the in situ formation of a trialkoxyhydrosilane and activation with a Lewis base, as further indicated by density functional theory studies. 1,3-Dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone (DMPU) was identified to be a suitable catalyst for this metal-free reduction, promoting the regio- and chemoselective reduction of aldehydes in ortho-position to phenols, despite the presence of vicinal ketones. The performance of pinacol-derived chlorohydrosilane in the reduction of salicylaldehydes was further observed to be superior to that of well-established commercially available chlorohydrosilanes.

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