13065-07-1 Usage
Explanation
Different sources of media describe the Explanation of 13065-07-1 differently. You can refer to the following data:
1. The chemical compound 2,7-Dimethyltetraline is composed of 10 carbon atoms and 14 hydrogen atoms.
2. 2,7-Dimethyltetraline belongs to the group of organic compounds known as tetralines, which are a type of polycyclic aromatic hydrocarbon.
3. The compound is in a liquid state and is colorless, making it difficult to see.
4. 2,7-Dimethyltetraline has a distinctive and recognizable aromatic smell.
5. 2,7-Dimethyltetraline serves as a starting material or building block in the synthesis of various other organic compounds.
6. In chemical reactions, 2,7-Dimethyltetraline can act as a ligand, which is a molecule that binds to a metal center, playing a role in metal-catalyzed reactions.
7. 2,7-Dimethyltetraline has potential uses in the production of various products, including pharmaceuticals, agrochemicals (chemicals used in agriculture), and other fine chemicals.
8. If not handled or stored correctly, 2,7-Dimethyltetraline can pose hazards, so it is essential to use caution when working with this compound.
Class of Compounds
Tetralines (Polycyclic Aromatic Hydrocarbons)
Physical State
Colorless Liquid
Aromatic Odor
Unique
Usage as Precursor
Synthesis of Organic Compounds
Role as Ligand
Metal-Catalyzed Reactions
Industrial Applications
Pharmaceuticals, Agrochemicals, and Fine Chemicals
Hazardous Nature
Proper Handling and Storage Required
Check Digit Verification of cas no
The CAS Registry Mumber 13065-07-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,6 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 13065-07:
(7*1)+(6*3)+(5*0)+(4*6)+(3*5)+(2*0)+(1*7)=71
71 % 10 = 1
So 13065-07-1 is a valid CAS Registry Number.
InChI:InChI=1/C12H16/c1-9-3-5-11-6-4-10(2)8-12(11)7-9/h3,5,7,10H,4,6,8H2,1-2H3
13065-07-1Relevant articles and documents
Weinstein,Fenselau
, p. 1463,1466 (1963)
Nickel-tungsten sulfide aromatic hydrocarbon hydrogenation catalysts synthesized in situ in a hydrocarbon medium
Sizova,Serdyukov,Maksimov
, p. 470 - 480 (2015/11/23)
Nickel-tungsten sulfide nanocatalysts for the hydrogenation of aromatic hydrocarbons (HCs) have been prepared by the in situ decomposition of a nickel thiotungstate precursor in a HC feedstock using 1-butyl-1-methylpiperidinium nickel thiotungstate complex [BMPip]2Ni[WS4]2 as the precursor. The in situ synthesized particles have been characterized by X-ray photoelectron spectroscopy and high-resolution transmission electron microscopy. It has been shown that the resulting Ni-W-S particles are nanoplates associated in multilayer agglomerates; the average length of the Ni-W-S particles is 6 nm; the average number of layers in the multilayer packaging is three. The catalytic activity of the synthesized catalysts has been studied in the hydrogenation of model mixtures of mono- and bicyclic aromatic HCs and in the conversion of dibenzothiophene in a batch reactor at a temperature of 350°C and a hydrogen pressure of 5.0 MPa. It has been shown that the studied catalysts can be used for the hydrofining of light cycle oil.
