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Trans-2-Methyldecalin(axial) is a chemical compound with the molecular formula C11H22, belonging to the alkyl-decalin class of organic compounds. It features a ten-carbon bicyclic structure with two methyl groups in a trans configuration, positioned on opposite sides of the decalin ring. The "axial" label denotes that one of the methyl groups is in an axial position, oriented perpendicular to the plane of the decalin ring.

4683-94-7

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4683-94-7 Usage

Uses

Used in Fragrance Production:
Trans-2-Methyldecalin(axial) is utilized as a key component in the production of fragrances, providing unique scents and enhancing the overall aroma of various products.
Used as an Industrial Solvent:
trans-2-Methyldecalin(axial) serves as a solvent in a range of industrial processes, facilitating the dissolution of various substances and enabling efficient manufacturing techniques.
Used in Organic Synthesis:
Trans-2-Methyldecalin(axial) acts as a building block in the synthesis of other organic compounds, contributing to the creation of new molecules with diverse applications across different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 4683-94-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,8 and 3 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4683-94:
(6*4)+(5*6)+(4*8)+(3*3)+(2*9)+(1*4)=117
117 % 10 = 7
So 4683-94-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H20/c1-9-5-4-7-10-6-2-3-8-11(9)10/h9-11H,2-8H2,1H3

4683-94-7Downstream Products

4683-94-7Relevant academic research and scientific papers

Synthesis of nickel-tungsten sulfide hydrodearomatization catalysts by the decomposition of oil-soluble precursors

Sizova,Kulikov,Onishchenko,Serdyukov,Maksimov

, p. 44 - 50 (2016/02/03)

Nickel-tungsten sulfide catalysts for the hydrogenation of aromatic hydrocarbons have been prepared by the in situ decomposition of an oil-soluble tungsten hexacarbonyl precursor in a hydrocarbon feedstock using oil-soluble nickel salt nickel(II) 2-ethylhexanoate as a source of nickel. The in situ synthesized Ni-W-S catalyst has been characterized by X-ray photoelectron spectroscopy. The activity of the resulting catalysts has been studied in the hydrogenation of bicyclic aromatic hydrocarbons and dibenzothiophene conversion in a batch reactor at a temperature of 350°C and a hydrogen pressure of 5.0 MPa. It has been shown that the optimum W: Ni molar ratio is 1: 2. Using the example of the hydrofining of feedstock with high sulfur and aromatics contents, it has been shown that the synthesized catalyst exhibits high activity in the hydrogenation of aromatic hydrocarbons.

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