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p-methoxyphenyltellurium trichloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

36309-68-9

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36309-68-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36309-68-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,3,0 and 9 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 36309-68:
(7*3)+(6*6)+(5*3)+(4*0)+(3*9)+(2*6)+(1*8)=119
119 % 10 = 9
So 36309-68-9 is a valid CAS Registry Number.

36309-68-9SDS

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 (4-methoxyphenyl)TeCl3

1.2 Other means of identification

Product number -
Other names (4-methoxyphenyl)tellurium trichloride

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:36309-68-9 SDS

36309-68-9Relevant academic research and scientific papers

Studies on nickel(II) and palladium(II) complexes with some tetraazamacrocycles containing tellurium

Rathee, Nitu,Verma, Krishan Kumar

, p. 325 - 333 (2012)

The synthesis of 10-membered and 12-membered tellurium-containing tetraazamacrocyclic complexes of divalent nickel and palladium by template condensation of diaryltellurium dichlorides, (aryl = p-hydroxyphenyl, 4-hydroxy-3-methyl-phenyl, p-methoxyphenyl)

Synthesis, Characterization and Antimicrobial Studies of Some New Tellurium(IV) Complexes Derived from 2-[(2-Hydroxyphenyl)imino methyl]-1-naphthol Schiff Base

Dalal, Mahak,Garg, Sapana,Kumar, Manish,Verma, K. K.

, p. 183 - 190 (2022/01/08)

This article reports the synthesis, characterization and antimicrobial screening of a tridentate 2-[(2-hydroxyphenyl)imino methyl]-1naphthol ligand (H2AP) and its organotellurium(IV) complexes. Structural characterization of the synthesized ligand and com

Some organotellurium(iv) complexes of 1-methyl-3-(p-tolylimino)indolin-2-one schiff base

KUMAR, MANISH,VERMA,GARG, SAPANA

, p. 1236 - 1244 (2021/06/09)

Six new hexa-coordinated organotellurium(IV) complexes of type RTeCl3 NMeIPT and R2TeCl2 NMeIPT (R = 4-hydroxyphenyl, 4- methoxyphenyl or 3-methy-4-hydroxyphenyl; NMeIPT(L) = Schiff base (1-methyl-3-(p-tolylimino)indolin-2-one) derived from condensation o

Solventless and mild procedure to prepare organotellurium(IV) compounds under microwave irradiation

Princival, Cleverson,Dos Santos, Alcindo A.,Comasseto, Jo?o V.

, p. 832 - 836 (2015/05/20)

Tellurium(IV) tetrachloride, p-methoxyphenyltellurium trichloride and the corresponding products of its reaction with alkynes were prepared under very mild reaction conditions, in absence of organic solvents and in short reaction times all assisted by mic

Tellurium derivatives of 3-acetyl-2,5-dimethylthiophene: Synthetic and structural aspects

Singh, Poornima,Chauhan, Ashok K.S.,Butcher, Ray J.,Duthie, Andrew

, p. 44 - 51 (2013/05/09)

Oxidative addition of α-bromo-3-acetyl-2,5-dimethylthiophene to elemental tellurium and aryltellurium(II) bromide provides direct routes to (2,5-dimethyl-3-thiophenoylmethyl)tellurium(IV) dibromides, (Me 2TpnCOCH2)2TeBrsu

Synthesis and properties of tellurinic anhydride-tellurone adducts

Oba, Makoto,Nishiyama, Kozaburo,Koguchi, Shinichi,Shimada, Shigeru,Ando, Wataru

supporting information, p. 6620 - 6623 (2013/12/04)

The synthesis and characterization of stable tellurinic anhydride-tellurone adducts are reported. Treatment of aryltellurinic anhydride with diaryl tellurone gave pentacyclotelluroxane consisting of two molecules each of the starting tellurium oxides. The bulky aromatic substituents attached to the tellurium atoms efficiently prevent further aggregation and enable full characterization using multinuclear (1H, 13C, and 125Te) NMR and IR spectroscopy as well as elemental analysis. For (TipTe)4(Tip2Te)2O10 (3TT, Tip = 2,4,6-triisopropylphenyl), the molecular structure was unambiguously determined by an X-ray crystallographic analysis. To estimate the dissociation energies of the tellurinic anhydride-tellurone adducts, density functional theory calculations were performed, and it was found that the adducts are highly stabilized by forming a four di-μ-oxo bridge structure.

Stereospecific chlorotelluration of terminal acetylenes

Chauhan, Ashok K.S.,Bharti, Swami N.,Srivastava, Ramesh C.,Butcher, Ray J.,Duthie, Andrew

experimental part, p. 75 - 81 (2012/06/01)

Chlorotelluration of terminal acetylenes, RCHCH (R = Ph, 1; 4-MeC 6H4, 2; t-Bu, 3) with aryltellurium trichlorides and TeCl4 in refluxing toluene affords (2-chloro-2-organylvinyl) tellurium(IV) dichlorides, Ar[R(Cl)CCH]TeC

Tellurium tetrachloride: an improved method of preparation

Petragnani, Nicola,Mendes, Samuel R.,Silveira, Claudio C.

, p. 2371 - 2372 (2008/09/18)

An efficient and practical synthesis of tellurium tetrachloride from elemental tellurium and sulfuryl chloride is described.

TELLURADIAZAPHOSPHETIDINES: PREPARATION AND SPECTROSCOPIC CHARACTERIZATION OF THE PN2Te RING

Chivers, Tristram,Rao, M. N. Sudheendra

, p. 197 - 200 (2007/10/02)

The reactions of Ph2PN2(SiMe3)3 with ArTeCl3 (Ar = C6H5, C6H4OMe-4, mesityl) in acetonitrile at 23 deg C produce Ph2P(NSiMe3)2TeCl2Ar, which are formulated as four-membered rings on the basis of analytical and NMR (1H, 31P, 125Te) spectroscopic data. Key

Facile Reaction of Te-Aryl Benzenecarbotelluroates, ArCOTeAr', with Methyl Iodide and Halogens

Singh, Harkesh B.,Sudha, Narasimhan

, p. 3735 - 3736 (2007/10/02)

Reaction of Te-aryl benzenecarbotelluroates of the type ArCOTeAr' (Ar=phenyl p-tolyl, p-bromophenyl; Ar'=phenyl, p-methoxyphenyl) with methyl iodide was found to give symmetrical telluronium salts, (1+)I(1-) in good yields.The reactivity of one of these benzene carbotelluroates towards halogens was also examined.

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