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116697-35-9

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116697-35-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 116697-35-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,6,9 and 7 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 116697-35:
(8*1)+(7*1)+(6*6)+(5*6)+(4*9)+(3*7)+(2*3)+(1*5)=149
149 % 10 = 9
So 116697-35-9 is a valid CAS Registry Number.

116697-35-9Relevant articles and documents

Shelton,J.R.,Henderson,J.N.

, p. 2185 - 2190 (1961)

Aromatic compound hydrogenation and hydrodeoxygenation method and application thereof

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Paragraph 0094-0095; 0114-0122, (2021/05/29)

The invention belongs to the technical field of medicines, and discloses an aromatic compound hydrogenation and hydrodeoxygenation method under mild conditions and application of the method in hydrogenation and hydrodeoxygenation reactions of the aromatic compounds and related mixtures. Specifically, the method comprises the following steps: contacting the aromatic compound or a mixture containing the aromatic compound with a catalyst and hydrogen with proper pressure in a solvent under a proper temperature condition, and reacting the hydrogen, the solvent and the aromatic compound under the action of the catalyst to obtain a corresponding hydrogenation product or/and a hydrodeoxygenation product without an oxygen-containing substituent group. The invention also discloses specific implementation conditions of the method and an aromatic compound structure type applicable to the method. The hydrogenation and hydrodeoxygenation reaction method used in the invention has the advantages of mild reaction conditions, high hydrodeoxygenation efficiency, wide substrate applicability, convenient post-treatment, and good laboratory and industrial application prospects.

Hydrogenolysis of lignin model compounds into aromatics with bimetallic Ru-Ni supported onto nitrogen-doped activated carbon catalyst

Hu, Yinghui,Jiang, Guangce,Xu, Guoqiang,Mu, Xindong

, p. 316 - 326 (2018/01/05)

Lignin is the most abundant and renewable resources for production of natural aromatics. In this paper, new bimetallic catalytic system of Ru and Ni supported onto nitrogen-doped activated carbon (Ru-Ni-AC/N) was developed and its performances on hydrogenolysis of lignin model compounds under mild reaction conditions (1.0 MPa, 230 °C, in aqueous) were investigated. The results indicate that Ru-Ni-AC/N was a highly active, selective and stable catalyst for the conversion of lignin model compounds into aromatics, e.g. phenol, benzene and their derivatives. As verified by BET, XRD, HRTEM, XPS, H2-TPR and ICP-MS, the strong synergistic effects between i) Ru and Ni and ii) metals and N-groups were contributed to its excellent aromatics selectivity. What's more, the introduction of electron rich N atoms on AC was beneficial to the stabilization of metal particles, which greatly enhanced the durability of the catalyst.

Ruthenium Nanoparticles Stabilized in Cross-Linked Dendrimer Matrices: Hydrogenation of Phenols in Aqueous Media

Maximov, Anton,Zolotukhina, Anna,Murzin, Vadim,Karakhanov, Edward,Rosenberg, Edward

, p. 1197 - 1210 (2015/04/14)

Novel catalysts consisting of ruthenium nanoparticles encapsulated in cross-linked matrices based on the poly(propylene imine) dendrimers of the 1st and 3rd generations have been synthesized with a narrow particle size distribution (3.8 and 1.0 nm, respectively). The resulting materials showed high activity for the hydrogenation of phenols in aqueous media (specific catalytic activity reached turnover frequencies of 2975h-1 with respect to hydrogen uptake). It has been shown that the use of water as a solvent leads to a 1.5 to 50-fold increase in the reaction rate depending upon the nature of the substrate. It has been established that unlike the traditional heterogeneous catalysts based on ruthenium, during the hydrogenation of dihydroxybenzenes, the hydrogenation rate decreases in the order: resorcinol>hydroquinoneacatechol. The maximum specific activity for resorcinol was a turnover frequency of 243150h-1 with respect to hydrogen uptake. The catalyst based on the dendrimer of the 3rd generation containing finer particles has significantly inferior activity to the catalyst based on the dendrimer of the 1st generation by virtue of steric factors, as well as the need for prereduction of the ruthenium oxide contained on the surface. These catalysts showed resistance to metal leaching and may be reused several times without loss of activity.

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