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DIISOPROPYLDITELLURIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 51112-73-3 Structure
  • Basic information

    1. Product Name: DIISOPROPYLDITELLURIDE
    2. Synonyms: DIISOPROPYLDITELLURIDE
    3. CAS NO:51112-73-3
    4. Molecular Formula: C6H14Te2
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 51112-73-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: DIISOPROPYLDITELLURIDE(CAS DataBase Reference)
    10. NIST Chemistry Reference: DIISOPROPYLDITELLURIDE(51112-73-3)
    11. EPA Substance Registry System: DIISOPROPYLDITELLURIDE(51112-73-3)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 51112-73-3(Hazardous Substances Data)

51112-73-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51112-73-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,1,1 and 2 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 51112-73:
(7*5)+(6*1)+(5*1)+(4*1)+(3*2)+(2*7)+(1*3)=73
73 % 10 = 3
So 51112-73-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H14Te2/c1-5(2)7-8-6(3)4/h5-6H,1-4H3

51112-73-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(propan-2-ylditellanyl)propane

1.2 Other means of identification

Product number -
Other names Diisopropylditellurid

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:51112-73-3 SDS

51112-73-3Relevant articles and documents

Divinyl ditellurides: synthesis and reactivity

Dabdoub, M. J.,Comasseto, J. V.

, p. 167 - 174 (1988)

Reaction of vinyl Grignard reagents with elemental tellurium followed by air oxidation furnished divinyl ditellurides in 58-68percent yield.When the intermediate bromomagnesium ethenetellurolat

Synthesis of bis(alkyltelluro)methanes and their complexation with cadmium(II)

Selvakumar,Singh,Nasim,Mathur

, p. 247 - 259 (2007/10/03)

A novel and convenient route for the synthesis of a series of bis(alkyltelluro)methanes (alkyl=elhyl, isopropyl, n-butyl and n-hexyl) is described by one pot methylene insertion reaction using dialkyl ditellurides, sodium borohydride and chloroform. The cadmium(II) complexes of bis(isopropyltelluro)methane were also synthesized. The bis(alkyltelluro)methanes were characterized by elemental analysis, 1H and 125Te NMR. The product of the complexation of bis(isopropyl telluro(methane with Cd(II) have been characterized by elemental analysis, 1H, TGA and FAB mass spectrometry. The dialkyltelluroether ligands may be useful in organic synthesis and their complexes with cadmium(II) can be considered a potential single source of metal-organic chemical vapor deposition (MOCVD) precursors for advanced electronic materials.

A convenient method for the preparation of dialkylditellurides and dialkyldiselenides

Li,Bao,Lue,Zhou

, p. 799 - 806 (2007/10/02)

Dialkylditellurides 3 and dialkyldiselenides 4 were prepared in high yields and in a one-pot procedure by the reduction of elemental tellurium and selenium with phenyl hydrazine in basic medium (NaOH/DMF) followed by treatment with organohalides.

A Novel Synthesis of Organic Tellurium Compounds by the Use of Electrochemically Generated Polytelluride-ions

Merkel, G.,Berge, H.,Jeroschewski, P.

, p. 467 - 478 (2007/10/02)

The cathodic polarisation of a tellurium electrode in aprotic solutions gives rise to polytelluride anions, which react with alkylhalides to the corresponding disubstituted ditellurides.By this method of electrosynthesis a number of organic ditellurides can be simply prepared and whithout danger.Dialkylditellurides of the general formula R-Te-Te-R (2a-r) can be produced with high yields.The reaction with α,ω-dihalides gives heterocycles, which involve one or two tellurium atoms in the ring (5a-d, 6-8).The electrochemical reduction of tellurium in the presence of methyliodid yields trimethyltelluroniumiodid (9).

THE PREPARATION OF DI-t-BUTYL DITELLURIDE AND DI-t-BUTYL TELLURIDE AND THE 125Te NMR AND MOESSBAUER SPECTRA OF SOME DIALKYL TELLURIDES AND DITELLURIDES

Jones, C.H.W.,Sharma, R.D.

, p. 61 - 70 (2007/10/02)

The synthesis of di-t-butyl ditelluride, t-Bu2Te2, an di-t-butyl telluride, t-Bu2Te, are reported together with that of di-(neo-hexyl) ditelluride.New syntheses of Me2Te2 and i-Pr2Te2 are presented.The high resolution 125Te NMR data and the Moessbauer data for these compounds are discussed.The use of tellurium-proton couplings in high resolution 125Te NMR spectra in assigning the resonances in mixed dialkyl ditellurides is also illustrated.

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