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CAS

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144810-06-0

Triisopropyl-(6-phenylsulfanyl-cyclohex-1-enyloxy)-silane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 144810-06-0 Structure

  • Basic information

    1. Product Name: Triisopropyl-(6-phenylsulfanyl-cyclohex-1-enyloxy)-silane
    2. Synonyms:
    3. CAS NO:144810-06-0
    4. Molecular Formula:
    5. Molecular Weight: 362.652
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 144810-06-0.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: Triisopropyl-(6-phenylsulfanyl-cyclohex-1-enyloxy)-silane(CAS DataBase Reference)
    10. NIST Chemistry Reference: Triisopropyl-(6-phenylsulfanyl-cyclohex-1-enyloxy)-silane(144810-06-0)
    11. EPA Substance Registry System: Triisopropyl-(6-phenylsulfanyl-cyclohex-1-enyloxy)-silane(144810-06-0)

  • 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: 144810-06-0(Hazardous Substances Data)

144810-06-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 144810-06-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,8,1 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 144810-06:
(8*1)+(7*4)+(6*4)+(5*8)+(4*1)+(3*0)+(2*0)+(1*6)=110
110 % 10 = 0
So 144810-06-0 is a valid CAS Registry Number.

144810-06-0Downstream Products

144810-06-0Relevant articles and documents

New Mild Methodology for the Synthesis of α-Phenylthio and α-Phenylseleno Ketones

Magnus, Philip,Rigollier, Pascal

, p. 6111 - 6114 (2007/10/02)

Treatment of trimethylsilyl enol ethers with the adduct 1, derived from chloramine-T and (PhS)2, gave good yields of α-phenylthioketones.The selenium version of this reagent 2 gave α-phenylselenoketones.

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