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naphthalen-1-yl(o-tolyl)sulfane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 127567-56-0 Structure
  • Basic information

    1. Product Name: naphthalen-1-yl(o-tolyl)sulfane
    2. Synonyms: naphthalen-1-yl(o-tolyl)sulfane
    3. CAS NO:127567-56-0
    4. Molecular Formula:
    5. Molecular Weight: 250.364
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 127567-56-0.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: naphthalen-1-yl(o-tolyl)sulfane(CAS DataBase Reference)
    10. NIST Chemistry Reference: naphthalen-1-yl(o-tolyl)sulfane(127567-56-0)
    11. EPA Substance Registry System: naphthalen-1-yl(o-tolyl)sulfane(127567-56-0)
  • 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: 127567-56-0(Hazardous Substances Data)

127567-56-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 127567-56-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,5,6 and 7 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 127567-56:
(8*1)+(7*2)+(6*7)+(5*5)+(4*6)+(3*7)+(2*5)+(1*6)=150
150 % 10 = 0
So 127567-56-0 is a valid CAS Registry Number.

127567-56-0Relevant articles and documents

Forging C-S Bonds through Nickel-Catalyzed Aryl Anhydrides with Thiophenols: Decarbonylation or Decarbonylation Accompanied by Decarboxylation

Zhou, Jing-Ya,Tao, Shou-Wei,Liu, Rui-Qing,Zhu, Yong-Ming

, p. 11891 - 11901 (2019)

A nickel-catalyzed decarbonylation or decarbonylation accompanied by decarboxylation cross-coupling reaction of aryl anhydrides with thiophenols as coupling partners was disclosed. This method is promoted by a commercially available, moisture-stable, and inexpensive nickel(II) precatalyst. The process can tolerate a variety of functional groups using ubiquitous aryl anhydrides as cross-coupling precursors to produce thioethers in moderate to excellent yields.

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