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1194813-40-5

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1194813-40-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1194813-40-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,4,8,1 and 3 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1194813-40:
(9*1)+(8*1)+(7*9)+(6*4)+(5*8)+(4*1)+(3*3)+(2*4)+(1*0)=165
165 % 10 = 5
So 1194813-40-5 is a valid CAS Registry Number.

1194813-40-5Relevant articles and documents

Cobalt-Nanoparticles Catalyzed Efficient and Selective Hydrogenation of Aromatic Hydrocarbons

Murugesan, Kathiravan,Senthamarai, Thirusangumurugan,Alshammari, Ahmad S.,Altamimi, Rashid M.,Kreyenschulte, Carsten,Pohl, Marga-Martina,Lund, Henrik,Jagadeesh, Rajenahally V.,Beller, Matthias

, p. 8581 - 8591 (2019/09/12)

The development of inexpensive and practical catalysts for arene hydrogenations is key for future valorizations of this general feedstock. Here, we report the development of cobalt nanoparticles supported on silica as selective and general catalysts for such reactions. The specific nanoparticles were prepared by assembling cobalt-pyromellitic acid-piperazine coordination polymer on commercial silica and subsequent pyrolysis. Applying the optimal nanocatalyst, industrial bulk, substituted, and functionalized arenes as well as polycyclic aromatic hydrocarbons are selectively hydrogenated to obtain cyclohexane-based compounds under industrially viable and scalable conditions. The applicability of this hydrogenation methodology is presented for the storage of H2 in liquid organic hydrogen carriers.

A stable and practical nickel catalyst for the hydrogenolysis of C-O bonds

Cui, Xinjiang,Yuan, Hangkong,Junge, Kathrin,Topf, Christoph,Beller, Matthias,Shi, Feng

, p. 305 - 310 (2017/01/24)

The selective hydrogenolysis of C-O bonds constitutes a key step for the valorization of biomass including lignin fragments. Moreover, this defunctionalization process offers the possibility of producing interesting organic building blocks in a straightforward manner from oxygenated compounds. Herein, we demonstrate the reductive hydrogenolysis of a wide variety of ethers including diaryl, aryl-alkyl and aryl-benzyl derivatives catalyzed by a stable heterogeneous NiAlOx catalyst in the presence of a Lewis acid (LA). The special feature of this catalyst system is the formation of substituted cyclohexanols from the corresponding aryl ether.

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