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5-hexenyl phenyl telluride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 113303-11-0 Structure
  • Basic information

    1. Product Name: 5-hexenyl phenyl telluride
    2. Synonyms: 5-hexenyl phenyl telluride
    3. CAS NO:113303-11-0
    4. Molecular Formula:
    5. Molecular Weight: 287.859
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 113303-11-0.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: 5-hexenyl phenyl telluride(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-hexenyl phenyl telluride(113303-11-0)
    11. EPA Substance Registry System: 5-hexenyl phenyl telluride(113303-11-0)
  • 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: 113303-11-0(Hazardous Substances Data)

113303-11-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 113303-11-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,3,0 and 3 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 113303-11:
(8*1)+(7*1)+(6*3)+(5*3)+(4*0)+(3*3)+(2*1)+(1*1)=60
60 % 10 = 0
So 113303-11-0 is a valid CAS Registry Number.

113303-11-0Downstream Products

113303-11-0Relevant articles and documents

A new, practical synthesis of organotellurium compounds from organic halides and silyl tellurides. Remarkable effects of polar solvents and leaving groups

Yamago, Shigeru,Iida, Kazunori,Yoshida, Jun-ichi

, p. 5061 - 5064 (2001)

Silyl tellurides react with organic halides to give the corresponding organotellurium compounds and silyl halides in good to excellent yields. Substitution proceeds in polar solvents, such as acetonitrile, but not in nonpolar solvents under identical conditions. The leaving group also plays a significant role, with alkyl bromides being the most reactive, alkyl chlorides less so and alkyl iodides the least reactive. After removal of the volatile silyl halides and solvent under vacuum, the essentially pure organotellurium compounds, which can be used directly as precursors for carbocations, carbanions, and carbon-centered radicals, were obtained.

Experimental and theoretical studies on formal σ-bond metathesis of silyl tellurides with alkyl halides

Yamago, Shigeru,Iida, Kazunori,Yoshida, Jun-ichi

, p. 664 - 670 (2008/02/06)

Silyl tellurides reacted with alkyl halides under mild thermal conditions to give the corresponding alkyl tellurides and silylhalides in good to excellent yields. Substitution took place much faster in polar solvents, such as acetonitrile, than that in no

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