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Ditelluride, bis(2-methylphenyl) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

36692-34-9

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36692-34-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36692-34-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,6,9 and 2 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 36692-34:
(7*3)+(6*6)+(5*6)+(4*9)+(3*2)+(2*3)+(1*4)=139
139 % 10 = 9
So 36692-34-9 is a valid CAS Registry Number.

36692-34-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name Bis(2-methylphenyl)ditelluride

1.2 Other means of identification

Product number -
Other names di-o-tolylditelluride

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:36692-34-9 SDS

36692-34-9Relevant academic research and scientific papers

Tellurides Bearing Sulfonamides as Novel Inhibitors of Leishmanial Carbonic Anhydrase with Potent Antileishmanial Activity

Angeli, Andrea,Etxebeste-Mitxeltorena, Mikel,Sanmartín, Carmen,Espuelas, Socorro,Moreno, Esther,Azqueta, Amaya,Parkkila, Seppo,Carta, Fabrizio,Supuran, Claudiu T.

, p. 4306 - 4314 (2020/05/25)

We report for the first time a novel series of tellurides bearing sulfonamide as selective and potent inhibitors of the β-class carbonic anhydrase (CA; EC 4.2.1.1) enzyme expressed in Leishmania donovani protozoa. Such derivatives showed high activity against axenic amastigotes, and among them, compound 5g (4-(((3,4,5-trimethoxyphenyl)tellanyl)methyl)benzenesulfonamide) showed an IC50 of 0.02 μM being highly selective for the parasites over THP-1 cells with a selectivity index of 300. The in vitro and in vivo toxicity experiments showed compound 5g to possess a safe profile and thus paving the way for tellurium-containing compounds as novel drug entities.

Platinum-Mediated Activation of Coordinated Organonitriles by Telluroethers in Tetrahydrofuran: Isolation, Structural Characterization, and Density Functional Theory Analysis of Intermediate Complexes

Kolay, Siddhartha,Wadawale, Amey,Nigam, Sandeep,Kumar, Mukesh,Majumder, Chiranjib,Das, Dasarathi,Jain, Vimal K.

supporting information, p. 11741 - 11750 (2015/12/31)

The reactions of [PtCl2(NCR)2] with telluroethers (ArAr′Te) in organic solvents have been investigated. The reactions in dichloromethane yield [PtCl2(TeArAr′)2], while those in tetrahydrofuran (THF) give different products depending on the steric demands of the aryl groups on tellurium, the molarity of the reactants, and the reaction conditions. The reactions between [PtCl2(PhCN)2] and TeArAr′ in 1:1 molar ratio at room temperature in THF yield several products, like [PtCl2(TeArAr′)2] (Ar/Ar′ = Ph/Ph, o-tol/Mes, Mes/Mes), [PtCl2(PhCN){NC(O)Ph[TeMes(o-tol)]}], and [PtCl2{NC(O)Ph(TeMes2)}2]. The reaction with TeMes2 in refluxing THF gave [PtCl2{NC(Ph)C4H7O}{NC(O)Ph(TeMes2)}] and [PtCl(TeMes2){Te(Mes)CH2C6H2Me2}], depending on the duration of heating. Reaction of [PtCl2(PhCN)2] with TeArMes afforded [PtCl2(TeArMes)2] (Ar = Ph, o-tol, and Mes), the formation of which decreased with increasing steric demand of the Ar group, together with [PtCl2{NC(O)Ph(TeArMes)}2]. The telluroether in the latter binds to nitrogen, and tellurium exists in the formal oxidation state of +4 (from XPS). The tellurium in these complexes exhibits secondary interactions with platinum (J(195Pt-125Te) = 309-347 Hz) and with the carbonyl oxygen. These complexes slowly dissociate in solution to give [PtCl2(TeMesAr){NC(O)Ph(TeMesAr)}], finally leading to the formation of [PtCl2(TeMesAr)2]. Molecular structures of trans-[PtCl2(PhCN){NC(O)Ph[TeMes(o-tol)]}], trans-[PtCl2{NC(O)Ph(TeMes2)}2], trans-[PtCl2{NC(Ph)C4H7O}{NC(O)Ph(TeMes2)}], trans-[PtCl2{NC(O)Ph[TeMes(o-tol)]}2], trans-[PtCl2(TeMes2){NC(O)Ph(TeMes2)}], trans-[PtCl2{NC(O)Me(TeMes2)}2], and [PtCl(Te-o-tol){NC(O)Ph}2] have been unambiguously established by single-crystal X-ray diffraction analyses. Density functional theory calculations for some of the complexes were performed, and geometrical parameters are in good agreement with the values obtained from X-ray analyses.

Cyclopalladation of telluro ether ligands: Synthesis, reactivity and structural characterization

Kolay, Siddhartha,Kumar, Mukesh,Wadawale, Amey,Das, Dasarathi,Jain, Vimal K.

supporting information, p. 16056 - 16065 (2015/01/09)

Treatment of [PdCl2(PhCN)2] with diaryl telluride in 1:2 molar ratio gave mononuclear palladium complexes, trans-[PdCl2(TeR2)2] (1) (R = Mes (1a) (Mes = 2,4,6-trimethylphenyl), Ph (1b), o-tol (1c) (o-tol = ortho-tolyl)). Reaction of [PdCl2(TeMes2)2] with one equivalent of [PdCl2(PhCN)2] or Na2PdCl4 with TeRR′ afforded chloro-bridged binuclear complexes, [Pd2(μ-Cl)2Cl2(TeRR′)2] (2) (R/R′ = Mes/Mes (2a); Mes/Ph (2b); Ph/Ph (2c)). A toluene-methanol solution of trans-[PdCl2(TeMes2)2] on refluxing for 30 minutes yielded a binuclear cyclopalladated complex, [Pd2(μ-Cl)2{CH2C6H2(4,6-Me2)TeMes)}2] (3). When the refluxing was prolonged, a mononuclear complex cis-[PdCl2{MesTeCH2C6H2(4,6-Me2)TeMes}] (4) was isolated. Treatment of palladium acetate with TeMes2 afforded an acetato-bridged analogue of 3, [Pd2(μ-OAc)2{CH2C6H2(4,6-Me2)TeMes}2] (5a) together with a very minor component, a tetranuclear complex, [Pd(μ-OAc)(μ-TeMes)]4 (6). This reaction with unsymmetrical tellurides, MesTeR, also gave cyclopalladated complexes [Pd2(μ-OAc)2{CH2C6H2(4,6-Me2)TeR}2] (R = o-tol (5b) and Ph (5c)) in which 2-methyl of the mesityl group of the telluride was exclusively metallated. The complex trans-[PdCl2(TeMes2)2] on refluxing in xylene gave palladium telluride, Pd7Te3. These complexes were characterized by elemental analyses, IR and NMR (1H, 13C and 125Te) spectroscopy. The molecular structures of trans-[PdCl2(TeMes2)2] (1a), [Pd2(μ-Cl)2Cl2(TeMes2)2]·2acetone (2a·2acetone), cis-[PdCl2{MesTeCH2C6H2(4,6-Me2)TeMes}] (4), [Pd2(μ-OAc)2{CH2C6H2(4,6-Me2)TeMes)}2]·toluene (5a·toluene), [Pd2(μ-OAc)2{CH2C6H2(4,6-Me2)Tetol-o}2] (5b) and [Pd(μ-OAc)(μ-TeMes)]4 (6) were established by single crystal X-ray diffraction analyses. The mononuclear complex 1a was isolated in two polymorphic forms each with the trans configuration. This journal is

An efficient one-pot synthesis of symmetrical diselenides or ditellurides from halides with CuO nanopowder/Se0 or Te0/base

Singh, Devender,Deobald, Anna M.,Camargo, Leandro R.S.,Tabarelli, Greice,Rodrigues, Oscar E.D.,Braga, Antonio L.

supporting information; experimental part, p. 3288 - 3291 (2010/09/30)

(Equation Presented). A CuO nanopowder-catalyzed coupling reaction of aryl, alkyl, and heteroaryl iodides with elemental selenium and tellurium takes place in the presence of KOH at 90 °C in DMSO. A wide range of substituted symmetrical diselenides and ditellurides were afforded with good to excellent yields.

Synthesis of a New Tellurium Heterocycle, 5H,7H-Dibenzotellurathiocin, and Isolation and Reactivity of Its Tellurathia Dication Salt

Fujihara, Hisashi,Takaguchi, Yutaka,Chiu, Jer-Jye,Erata, Tomoki,Furukawa, Naomichi

, p. 151 - 154 (2007/10/02)

A new heterocycle containing tellurium and sulfur atoms, 5H,7H-dibenzotellurathiocin (1), has been synthesized.The transannular bond formation between tellurium and sulfur atoms was found in the reaction of 1 with concd H2SO4 by 1H, 13C, and 125

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