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CAS

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138502-79-1

4-trichlorotellurio-5-chlorocyclohexene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 138502-79-1 Structure

  • Basic information

    1. Product Name: 4-trichlorotellurio-5-chlorocyclohexene
    2. Synonyms:
    3. CAS NO:138502-79-1
    4. Molecular Formula:
    5. Molecular Weight: 349.542
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 138502-79-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-trichlorotellurio-5-chlorocyclohexene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-trichlorotellurio-5-chlorocyclohexene(138502-79-1)
    11. EPA Substance Registry System: 4-trichlorotellurio-5-chlorocyclohexene(138502-79-1)

  • 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: 138502-79-1(Hazardous Substances Data)

138502-79-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138502-79-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,5,0 and 2 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 138502-79:
(8*1)+(7*3)+(6*8)+(5*5)+(4*0)+(3*2)+(2*7)+(1*9)=131
131 % 10 = 1
So 138502-79-1 is a valid CAS Registry Number.

138502-79-1Upstream product

138502-79-1Downstream Products

138502-79-1Relevant articles and documents

TeCl4 in organic synthesis. Elimination reactions

Albeck, Michael,Tamary, Tova

, p. 35 - 42 (1991)

TeCl4 has been shown to react smoothly with unsaturated or halogenated cyclohydrocarbons.With cyclohexene, alkylcyclohexenes, halogenocyclohexenes, halogenocyclohexanes or unsaturated polycyclic compounds at elevated temperatures (ca 80 deg C), aromatization takes place as the only process, whereas at room temperature, addition products of halogenation or halogenotelluration are also formed.With conjugated dienes only chlorine-containing products are obtained with TeCl4, whereas dienes with separated double bonds undergo addition of TeCl4 to the double bond.An ionicpathway for the addition and aromatization reactions is suggested.

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