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151710-78-0

((Z)-3-Iodo-but-2-enyloxy)-triphenyl-silane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 151710-78-0 Structure

  • Basic information

    1. Product Name: ((Z)-3-Iodo-but-2-enyloxy)-triphenyl-silane
    2. Synonyms:
    3. CAS NO:151710-78-0
    4. Molecular Formula:
    5. Molecular Weight: 456.398
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 151710-78-0.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: ((Z)-3-Iodo-but-2-enyloxy)-triphenyl-silane(CAS DataBase Reference)
    10. NIST Chemistry Reference: ((Z)-3-Iodo-but-2-enyloxy)-triphenyl-silane(151710-78-0)
    11. EPA Substance Registry System: ((Z)-3-Iodo-but-2-enyloxy)-triphenyl-silane(151710-78-0)

  • 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: 151710-78-0(Hazardous Substances Data)

151710-78-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 151710-78-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,7,1 and 0 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 151710-78:
(8*1)+(7*5)+(6*1)+(5*7)+(4*1)+(3*0)+(2*7)+(1*8)=110
110 % 10 = 0
So 151710-78-0 is a valid CAS Registry Number.

151710-78-0Downstream Products

151710-78-0Relevant articles and documents

Synthesis of Silicon Substituted Cyclopropylmethyl Alcohols in Optically Active Form via Asymmetric Simmons-Smith Reaction of γ-Silicon Substituted Allylic Alcohols

Ukaji, Yutaka,Sada, Kazunori,Inomata, Katsuhiko

, p. 1227 - 1230 (1993)

Optically active silicon substituted cyclopropyl methyl alcohols were synthesized through asymmetric Simmons-Smith reaction; that is, the reaction of γ-silicon substituted allylic alcohols with diethylzinc and diiodomethane utilizing (+)-diethyl tartrate

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