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2-iodo-3-phenylthiophene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

58267-81-5

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58267-81-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58267-81-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,2,6 and 7 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 58267-81:
(7*5)+(6*8)+(5*2)+(4*6)+(3*7)+(2*8)+(1*1)=155
155 % 10 = 5
So 58267-81-5 is a valid CAS Registry Number.

58267-81-5Relevant academic research and scientific papers

IODONIUM ANALOGS AS INHIBITORS OF NADPH OXIDASES AND OTHER FLAVIN DEHYDROGENASES; FORMULATIONS THEREOF; AND USES THEREOF

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Paragraph 0137, (2015/11/17)

Disclosed herein are novel iodonium analogs having anticancer and anti-inflammatory activity.

An efficient and regioselective iodination of electron-rich aromatic compounds using N-chlorosuccinimide and sodium iodide

Yamamoto, Takuya,Toyota, Kozo,Morita, Noboru

experimental part, p. 1364 - 1366 (2010/05/03)

An efficient and regioselective method for iodination of electron-rich aromatic compounds was found using N-chlorosuccinimide and sodium iodide in AcOH with short reaction times. This method is also applicable to non-benzenoid aromatic or heteroaromatic c

Polymer-Supported Synthesis of Regioregular Head-to-Tail-Coupled Oligo(3-arylthiophene)s Utilizing a Traceless Silyl Linker

Briehn, Christoph A.,Kirschbaum, Thomas,Baeuerle, Peter

, p. 352 - 359 (2007/10/03)

The solid-phase synthesis of regioregular head-to-tail-coupled oligo(3-arylthiophene)s has been achieved in high yield and purity by using a traceless silyl ether linkage. In the first step, the solution-phase synthesis of this class of conjugated oligomers was investigated. Benzyl alcohol was chosen to serve as a mimic for the anchoring group of the hydroxymethyl-substituted polystyrene matrix. The development of a novel regioselective iodination process for silyl-protected thiophenes faciliates the successful application of the solution-phase protocol to the solid phase. Satisfactory loading was obtained by reaction of chlorosilyl-functionalized 3-arylthiophene with hydroxymethyl polystyrene in the presence of imidazole. The suitability of the following iterative halogenation and Suzuki cross-coupling sequence is illustrated by the preparation of a quater(3-arylthiophene), the first regioregular head-to-tail-coupled oligothiophene that is synthesized on solid support. Removal of the conjugated oligomers from the solid support could be effectively achieved by treatment with tetrabutylammonium fluoride.

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