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1-(4-Methoxy-phenyl)-3,3-bis-methylsulfanyl-propan-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 156944-07-9 Structure
  • Basic information

    1. Product Name: 1-(4-Methoxy-phenyl)-3,3-bis-methylsulfanyl-propan-1-ol
    2. Synonyms: 1-(4-Methoxy-phenyl)-3,3-bis-methylsulfanyl-propan-1-ol
    3. CAS NO:156944-07-9
    4. Molecular Formula:
    5. Molecular Weight: 258.406
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 156944-07-9.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: 1-(4-Methoxy-phenyl)-3,3-bis-methylsulfanyl-propan-1-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(4-Methoxy-phenyl)-3,3-bis-methylsulfanyl-propan-1-ol(156944-07-9)
    11. EPA Substance Registry System: 1-(4-Methoxy-phenyl)-3,3-bis-methylsulfanyl-propan-1-ol(156944-07-9)
  • 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: 156944-07-9(Hazardous Substances Data)

156944-07-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 156944-07-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,9,4 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 156944-07:
(8*1)+(7*5)+(6*6)+(5*9)+(4*4)+(3*4)+(2*0)+(1*7)=159
159 % 10 = 9
So 156944-07-9 is a valid CAS Registry Number.

156944-07-9Relevant articles and documents

Facile One Pot Thermal Dehydration and Dethioacetalization of β-Hydroxydithioacetals with Dimethyl sulphoxide: Synthesis of α,β-Unsaturated Aldehydes

Rao, Ch. Srinivasa,Chandrasekharam, M.,Patro, Balaram,Ila, Hiriyakkanavar,Junjappa, Hiriyakkanavar

, p. 5783 - 5794 (1994)

The acyclic and cyclic β-hydroxydithioacetals 3a-m and 4a-b obtained by sodium borohydride reduction (or Grignard addition) of the corresponding β-oxodithioacetals 2a-m are shown to undergo facile one pot thermal dehydration and dethioacetalization in the presence of dimethyl sulphoxide to afford the corresponding ene- and polyene aldehydes 5a-m and 6a-b in good yields.The probable mechanism of dethioacetalization with dimethyl sulphoxide has also been discussed.

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