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496-10-6

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496-10-6 Usage

Definition

ChEBI: An ortho-fused bicyclic hydrocarbon comprising of a cyclohexane ring fused onto a cyclopentane ring.

Check Digit Verification of cas no

The CAS Registry Mumber 496-10-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,9 and 6 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 496-10:
(5*4)+(4*9)+(3*6)+(2*1)+(1*0)=76
76 % 10 = 6
So 496-10-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H16/c1-2-5-9-7-3-6-8(9)4-1/h8-9H,1-7H2/t8-,9+

496-10-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name hydrindane

1.2 Other means of identification

Product number -
Other names dihydroindene

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:496-10-6 SDS

496-10-6Relevant articles and documents

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.

Oxygen-Deficient Tungsten Oxide as Versatile and Efficient Hydrogenation Catalyst

Song, Jiajia,Huang, Zhen-Feng,Pan, Lun,Zou, Ji-Jun,Zhang, Xiangwen,Wang, Li

, p. 6594 - 6599 (2015/11/18)

Heterogeneous hydrogenation is one of the most important industrial operations, and reduced metals (mostly noble metals and a few inexpensive metals) generally serve as the catalyst to activate molecular H2. Herein we report oxygen-deficient tungsten oxide, such as WO2.72, is a versatile and efficient catalyst for the hydrogenation of linear olefins, cyclic olefins, and aryl nitro groups, with obvious advantages compared with non-noble metal nickel catalyst from the aspect of activity and selectivity. Density functional theory calculations prove the oxygen-deficient surface activates H2 very easily in both kinetics and thermodynamics. Testing on several oxygen-deficient tungsten oxides shows a linear dependence between the hydrogenation activity and oxygen vacancy concentration. Tungsten is earth-abundant, and WO2.72 can be synthesized in large scale using a low-cost procedure, which provides an ideal catalyst for industrial application. Because oxygen vacancy is a common characteristic of many metal oxides, the findings in this work may be extended to other metal oxides and thus provide the possibility for exploring a new type of hydrogenation catalyst.

Catalytic compositions and methods for asymmetric allylic alkylation

-

, (2008/06/13)

Complexes of a selected class of chiral ligands with molybdenum, tungsten or chromium, preferably molybdenum, are effective as catalysts in highly enantioselective and regioselective alkylation of allylic substrates.

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