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3178-23-2

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3178-23-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3178-23-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,7 and 8 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3178-23:
(6*3)+(5*1)+(4*7)+(3*8)+(2*2)+(1*3)=82
82 % 10 = 2
So 3178-23-2 is a valid CAS Registry Number.

3178-23-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name cyclohexylmethylcyclohexane

1.2 Other means of identification

Product number -
Other names Cyclohexane,1,1'-methylenebis

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3178-23-2 SDS

3178-23-2Relevant articles and documents

One-pot catalytic reaction to produce high-carbon-number dimeric deoxygenated hydrocarbons from lignin-derived monophenyl vanillin using Al2O3-cogelled Ru nanoparticles

Yati, Indri,Dwiatmoko, Adid Adep,Yoon, Ji Sun,Choi, Jae-Wook,Suh, Dong Jin,Jae, Jungho,Ha, Jeong-Myeong

, p. 243 - 250 (2016)

Al2O3-cogelled Ru nanoparticle (Ru@Al) catalyst was prepared by a one-pot in-situ alumina gelation method using a PVP-stabilized Ru colloid solution. The Ru@Al catalyst exhibited excellent catalytic activity during the liquid-phase hydrodeoxygenation of vanillin, demonstrating 100% conversion, as well as significantly higher yields of fully deoxygenated compounds compared to other conventional alumina-supported Ru catalysts. We also observed better selectivity to deoxygenated dimers with the Ru@Al catalyst. The improved catalytic selectivity was attributed to the hypothesized three-dimensional structures of Al2O3 surrounding the Ru nanoparticles, which improved the two-step reaction, containing the dimerization of the phenolic compounds and the hydrodeoxygenation of phenolic dimers to produce deoxygenated high-carbon-number hydrocarbons.

Fabricating nickel phyllosilicate-like nanosheets to prepare a defect-rich catalyst for the one-pot conversion of lignin into hydrocarbons under mild conditions

Cao, Meifang,Chen, Bo,He, Chengzhi,Ouyang, Xinping,Qian, Yong,Qiu, Xueqing

supporting information, p. 846 - 857 (2022/02/09)

The one-pot conversion of lignin biomass into high-grade hydrocarbon biofuels via catalytic hydrodeoxygenation (HDO) holds significant promise for renewable energy. A great challenge for this route involves developing efficient non-noble metal catalysts to obtain a high yield of hydrocarbons under relatively mild conditions. Herein, a high-performance catalyst has been prepared via the in situ reduction of Ni phyllosilicate-like nanosheets (Ni-PS) synthesized by a reduction-oxidation strategy at room temperature. The Ni-PS precursors are partly converted into Ni0 nanoparticles by in situ reduction and the rest remain as supports. The Si-containing supports are found to have strong interactions with the nickel species, hindering the aggregation of Ni0 particles and minimizing the Ni0 particle size. The catalyst contains abundant surface defects, weak Lewis acid sites and highly dispersed Ni0 particles. The catalyst exhibits excellent catalytic activity towards the depolymerization and HDO of the lignin model compound, 2-phenylethyl phenyl ether (PPE), and the enzymatic hydrolysis of lignin under mild conditions, with 98.3% cycloalkane yield for the HDO of PPE under 3 MPa H2 pressure at 160 °C and 40.4% hydrocarbon yield for that of lignin under 3 MPa H2 pressure at 240 °C, and its catalytic activity can compete with reported noble metal catalysts.

The solvent determines the product in the hydrogenation of aromatic ketones using unligated RhCl3as catalyst precursor

Bartling, Stephan,Chakrabortty, Soumyadeep,De Vries, Johannes G.,Kamer, Paul C. J.,Lund, Henrik,Müller, Bernd H.,Rockstroh, Nils

, p. 7608 - 7616 (2021/12/13)

Alkyl cyclohexanes were synthesized in high selectivity via a combined hydrogenation/hydrodeoxygenation of aromatic ketones using ligand-free RhCl3 as pre-catalyst in trifluoroethanol as solvent. The true catalyst consists of rhodium nanoparticles (Rh NPs), generated in situ during the reaction. A range of conjugated as well as non-conjugated aromatic ketones were directly hydrodeoxygenated to the corresponding saturated cyclohexane derivatives at relatively mild conditions. The solvent was found to be the determining factor to switch the selectivity of the ketone hydrogenation. Cyclohexyl alkyl-alcohols were the products using water as a solvent.

Selective hydrogenation of lignin-derived compounds under mild conditions

Chen, Lu,Van Muyden, Antoine P.,Cui, Xinjiang,Laurenczy, Gabor,Dyson, Paul J.

supporting information, p. 3069 - 3073 (2020/06/17)

A key challenge in the production of lignin-derived chemicals is to reduce the energy intensive processes used in their production. Here, we show that well-defined Rh nanoparticles dispersed in sub-micrometer size carbon hollow spheres, are able to hydrogenate lignin derived products under mild conditions (30 °C, 5 bar H2), in water. The optimum catalyst exhibits excellent selectivity and activity in the conversion of phenol to cyclohexanol and other related substrates including aryl ethers.

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