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bis(benzenethio)tellurium(II) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75264-81-2

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75264-81-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75264-81-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,2,6 and 4 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 75264-81:
(7*7)+(6*5)+(5*2)+(4*6)+(3*4)+(2*8)+(1*1)=142
142 % 10 = 2
So 75264-81-2 is a valid CAS Registry Number.

75264-81-2Relevant academic research and scientific papers

Kinetics and mechanism of the nucleophilic substitution of tellurium(II) dialkanethiolates, Te(SR1)2 with thiols, HSR2

Fleischer, Holger

, p. 815 - 825 (2007/10/03)

The equilibrium reaction between tellurium(II) dithiolates and thiols, Te(SR1)2 + 2 HSR2 ? Te(SR 2)2 + 2 HSR1 was studied by means of 1H- and 125Te NMR spectroscopy and ab initio quantum chemical methods. It was found that the reaction is catalyzed by Bronsted acids and bases, the catalytic activity corresponding to the strength of the respective acid or base. Investigation of the initial step of the reaction, Te(SR1)2 + HSR2 ? Te(SR 1)(SR2) + HSR1, showed it to proceed according to first order kinetics for Te(SR1)2, HSR2 and for the catalyst. Ab initio geometry optimizations and frequency calculations suggest [Te(SR1)(HSR1)(HSR2)]+ and [Te(SR1)2(SR2)]- to be stable intermediates and not transition states in the acid and base catalyzed reactions, respectively. The reaction hence proceeds via an additional elimination rather than an SN2 mechanism. The catalytic activity displayed by acids and bases can be applied to reduce the temperature in synthesis of thermally labile tellurium(II) dithiolates. Copyright Taylor & Francis Inc.

TELLURIUM TETRACHLORIDE AS A MILD DEPROTECTION REAGENT FOR ACETALS AND THIOACETALS

Tani, Hiroyuki,Inamasu, Tokuo,Masumoto, Kazunori,Tamura, Rui,Shimizu, Hiroshi,Suzuki, Hitomi

, p. 261 - 266 (2007/10/02)

On treatment with tellurium tetrachloride in dichloromethane at room temperature, acetals and thioacetals are easily cleaved to regenerate original carbonyl compounds in good yields.

REACTION OF TETRAKIS(2,2,3,3-TETRAFLUOROPROPOXY)TELLURANE WITH THIOPHENOLS. BIS(ARYLTHIO)TELLURIUMS

Stukalo, E. A.,Yur'eva, E. M.,Markovskii, L. N.

, p. 301 - 303 (2007/10/02)

In the reaction of tetrakis(2,2,3,3-tetrafluoropropoxy)tellurane and tellurium tetrachloride with thiophenols the latter have a reducing action on the Te(IV) compounds.As a result bis-(arylthio)-telluriums and diaryl disulfides are formed.

MERCAPTO ACID COMPOUNDS OF TELLURIUM(II): STABILIZATION OF TELLURIUM-SULFUR BONDED COMPOUNDS VIA INTRAMOLECULAR CHELATION

Gardner, Sylvia A.

, p. 363 - 370 (2007/10/02)

A series of tellurium(II) compounds of general formula (RS)2Te (R = C6H5-, 2-C10H7-, HOOCCH2CH2-, HOOCCH(Me)-, HOOCCH2-, 2-(HOOC)C6H4-, HOOCCH2CH(COOH)-, NaOOCCH2CH2-, NH4OOCCH2CH2-) have been prepared and characterized.The tellurium compounds containing

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