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3877-19-8

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3877-19-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3877-19-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,7 and 7 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3877-19:
(6*3)+(5*8)+(4*7)+(3*7)+(2*1)+(1*9)=118
118 % 10 = 8
So 3877-19-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H14/c1-9-6-7-10-4-2-3-5-11(10)8-9/h2-5,9H,6-8H2,1H3/t9-/m0/s1

3877-19-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-1,2,3,4-tetrahydronaphthalene

1.2 Other means of identification

Product number -
Other names 2-Methyltetraline

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:3877-19-8 SDS

3877-19-8Relevant articles and documents

A new precursor for synthesis of nickel-tungsten sulfide aromatic hydrogenation catalyst

Serdyukov,Kniazeva,Sizova,Zubavichus,Dorovatovskii,Maximov

, (2021/01/18)

The unsupported NiWS-catalyst was obtained from the precursor [Ph3S]2Ni(WS4)2 in a hydrocarbon medium (in situ) for hydrogenation bicyclic aromatic compounds. The precursor [Ph3S]2Ni(WS4)2 and the catalyst prepared on its basis were studied by the X-ray diffraction and X-ray absorption methods, XPS and TEM. It was found that the new catalyst formed in situ contains tungsten sulfide and nickel sulfide nanophases. Tungsten sulfide, which has a layered structure, partially forms an insertion compound with nickel that enters between the WS2 layers and bonds covalently to sulfur. The proposed catalyst has proved to be active in the hydrodearomatization processes of model aromatic compounds (naphthalene, methylnaphthalenes) and exhibited the maximum selectivity with the formation of decalins compared to other earlier studied catalysts formed from other precursors in the reaction medium.

Hydroconversion of 2-methylnaphtalene and dibenzothiophene over sulfide catalysts in the presence of water under CO pressure

Glotov, A. P.,Karakhanov, E. A.,Maximov, A. L.,Vutolkina, A. V.

, p. 280 - 288 (2020/04/17)

Unsupported highly dispersed nanosized catalysts based on transition metal sulfides were prepared insitu, in water-oil emulsions, by high-temperature decomposition of oil soluble metal precursors using elemental sulfur as sulfiding agent. Their catalytic activity was tested in hydroconversion of 2-methylnaphtalene and dibenzothiophene at 380 °C under H2 pressure of 5 MPa. In addition, the catalysts were tested in the same reactions in the CO?H2O medium (p(CO) = 5 MPa, the CO: H2O molar ratio was 2: 1, ω(H2O) = 20 wt.%) in which hydrogen is formed through a water gas shift reaction (WGSR). Unsupported Ni?Mo-sulfide catalysts were found to be the most active compared to catalysts supported on alumina. Transmission electron microscopy served to investigate the structure and determine general geometric characteristics of Ni?Mo?S particles formed in toluene—water medium by decomposition of transition metal naphthenates and hexacarbonyls in the presence of elemental sulfur under CO pressure. The method described in this study enables one to synthesize nanosized catalysts with a high content of active sulfide phase.

Effect of Composition of Cobalt-Molybdenum-Containing Sulfonium Thiosalts on the Hydrogenation Activity of Nanosized Catalysts In Situ Synthesized on Their Basis

Knyazeva,Panyukova,Kuchinskaya,Kulikov,Maximov

, p. 1285 - 1292 (2019/12/28)

Abstract: Cobalt-molybdenum-containing thiosalts with different composition of the sulfonium cation are prepared. The activities of sulfide catalysts in situ synthesized on their basis in the hydrogenation of substituted naphthalenes are compared. It is shown that the sulfonium cation composition affects the morphology of the sulfide particles and the phase composition of the catalyst. It is demonstrated that the conversion of model alkyl-substituted bicyclic aromatic hydrocarbons is higher in the presence of the catalyst prepared from the phenylsulfonium thiosalt.

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