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17908-86-0

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17908-86-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17908-86-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,9,0 and 8 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 17908-86:
(7*1)+(6*7)+(5*9)+(4*0)+(3*8)+(2*8)+(1*6)=140
140 % 10 = 0
So 17908-86-0 is a valid CAS Registry Number.

17908-86-0Relevant articles and documents

Enhanced catalytic activity of self-assembled-monolayer-capped gold nanoparticles

Taguchi, Tomoya,Isozaki, Katsuhiro,Miki, Kazushi

, p. 6462 - 6467 (2012)

An unprecedented substrate-selective catalytic enhancement effect of an alkanethiol-self-assembled monolayer (SAM) on Au nanoparticles (AuNPs) is reported. In the supported 2D-array of AuNPs, the alkanethiol-SAM acts as a protein-like soft reaction space

Phosphirenium ions as masked phosphenium Catalysts: Mechanistic evaluation and application in synthesis

Gasperini, Danila,Neale, Samuel E.,Mahon, Mary F.,MacGregor, Stuart A.,Webster, Ruth L.

, p. 5452 - 5462 (2021/06/01)

The utilization of phosphirenium ions is presented; optimized and broadened three-membered ring construction is described together with the use of these ions as efficient pre-catalysts for metal-free carbonyl reduction with silanes. Full characterization of the phosphirenium ions is presented, and initial experimental and computational mechanistic studies indicate that these act as a "masked phosphenium"source that is accessed via ring opening. Catalysis proceeds via associative transfer of {Ph2P+} to a carbonyl nucleophile, Ha'SiR3 bond addition over the C=O group, and associative displacement of the product by a further equivalent of the carbonyl substrate, which completes the catalytic cycle. A competing off-cycle process leading to vinyl phosphine formation is detailed for the hydrosilylation of benzophenone for which an inverse order in [silane] is observed. Experimentally, the formation of side products, including off-cycle vinyl phosphine, is favored by electrondonating substituents on the phosphirenium cation, while catalytic hydrosilylation is promoted by electron-withdrawing substituents. These observations are rationalized in parallel computational studies.

Photoactivated silicon-oxygen and silicon-nitrogen heterodehydrocoupling with a commercially available iron compound

Cibuzar, Michael P.,Hammerton, James,Reuter, Matthew B.,Waterman, Rory

supporting information, p. 2972 - 2978 (2020/03/13)

Silicon-oxygen and silicon-nitrogen heterodehydrocoupling catalyzed by the commercially available cyclopentadienyl dicarbonyl iron dimer [CpFe(CO)2]2 (1) under photochemical conditions is reported. Reactions between alcohols and PhSi

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