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CAS

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174967-71-6

2-(1,2,3,4,5,6,7,8-octahydronaphthalen-1-yloxy)ethyl phenyl sulfoxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 174967-71-6 Structure

  • Basic information

    1. Product Name: 2-(1,2,3,4,5,6,7,8-octahydronaphthalen-1-yloxy)ethyl phenyl sulfoxide
    2. Synonyms:
    3. CAS NO:174967-71-6
    4. Molecular Formula:
    5. Molecular Weight: 304.453
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 174967-71-6.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: 2-(1,2,3,4,5,6,7,8-octahydronaphthalen-1-yloxy)ethyl phenyl sulfoxide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(1,2,3,4,5,6,7,8-octahydronaphthalen-1-yloxy)ethyl phenyl sulfoxide(174967-71-6)
    11. EPA Substance Registry System: 2-(1,2,3,4,5,6,7,8-octahydronaphthalen-1-yloxy)ethyl phenyl sulfoxide(174967-71-6)

  • 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: 174967-71-6(Hazardous Substances Data)

174967-71-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 174967-71-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,4,9,6 and 7 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 174967-71:
(8*1)+(7*7)+(6*4)+(5*9)+(4*6)+(3*7)+(2*7)+(1*1)=186
186 % 10 = 6
So 174967-71-6 is a valid CAS Registry Number.

174967-71-6Downstream Products

174967-71-6Relevant articles and documents

Cyclopentannulation by an iterative process of sequential Claisen rearrangement and enyne radical closure: Routes to triquinane and propellane systems and use in the synthesis of (±)-ceratopicanol

Clive,Magnuson,Manning,Mayhew

, p. 2095 - 2108 (1996)

Cycloalkenyl acetylenes 4, which are easily prepared from allylic alcohols by Claisen rearrangement and homologation (1 → 4), generally undergo radical cyclization (4 → 6) on treatment with stannyl radicals. The products (6) can themselves be converted in

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