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2-(4-iodophenyl)-1,3-dithiolane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1610009-75-0

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1610009-75-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1610009-75-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,1,0,0,0 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1610009-75:
(9*1)+(8*6)+(7*1)+(6*0)+(5*0)+(4*0)+(3*9)+(2*7)+(1*5)=110
110 % 10 = 0
So 1610009-75-0 is a valid CAS Registry Number.

1610009-75-0Relevant academic research and scientific papers

One-pot two-step conversion of aromatic carboxylic acids and esters to aromatic aldehydes via indium-catalyzed reductive thioacetalization and desulfurization

Sakai, Norio,Minato, Kohei,Ogiwara, Yohei

, p. 4563 - 4567 (2017)

Described herein is that a new approach to a one-pot two-step conversion of aromatic carboxylic acids/esters to aromatic aldehydes, in which indium(III) iodide effectively catalyzes both the first reductive thioacetalization of carboxylic acids and a subsequent desulfurization of the in-situ formed thioacetal intermediates leading to aldehydes.

Indium-Catalyzed Reductive Dithioacetalization of Carboxylic Acids with Dithiols: Scope, Limitations, and Application to Oxidative Desulfurization

Nishino, Kota,Minato, Kohei,Miyazaki, Takahiro,Ogiwara, Yohei,Sakai, Norio

, p. 3659 - 3665 (2017/04/11)

In this study an InI3-TMDS (1,1,3,3-tetramethyldisiloxane) reducing system effectively catalyzed the reductive dithioacetalization of a variety of aromatic and aliphatic carboxylic acids with 1,2-ethanedithiol or 1,3-propanedithiol leading to the one-pot preparation of either 1,3-dithiolane derivatives or a 1,3-dithiane derivative. Also, the intact indium catalyst continuously catalyzed the subsequent oxidative desulfurization of an in situ formed 1,3-dithiolane derivative, which led to the preparation of the corresponding aldehydes.

A collection of fullerenes for synthetic access toward oriented charge-transfer cascades in triple-channel photosystems

Bolag, Altan,Lopez-Andarias, Javier,Lascano, Santiago,Soleimanpour, Saeideh,Atienza, Carmen,Sakai, Naomi,Martin, Nazario,Matile, Stefan

supporting information, p. 4890 - 4895 (2014/05/20)

The development of synthetic methods to build complex functional systems is a central and current challenge in organic chemistry. This goal is important because supramolecular architectures of highest sophistication account for function in nature, and synthetic organic chemistry, contrary to high standards with small molecules, fails to deliver functional systems of similar complexity. In this report, we introduce a collection of fullerenes that is compatible with the construction of multicomponent charge-transfer cascades and can be placed in triple-channel architectures next to stacks of oligothiophenes and naphthalenediimides. For the creation of this collection, modern fullerene chemistry - methanofullerenes and 1,4-diarylfullerenes - is combined with classical Nierengarten-Diederich-Bingel approaches.

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