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518062-89-0

6-phenylethynyl-pyran-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 518062-89-0 Structure

  • Basic information

    1. Product Name: 6-phenylethynyl-pyran-2-one
    2. Synonyms: 6-phenylethynyl-pyran-2-one
    3. CAS NO:518062-89-0
    4. Molecular Formula:
    5. Molecular Weight: 196.205
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 518062-89-0.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: 6-phenylethynyl-pyran-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-phenylethynyl-pyran-2-one(518062-89-0)
    11. EPA Substance Registry System: 6-phenylethynyl-pyran-2-one(518062-89-0)

  • 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: 518062-89-0(Hazardous Substances Data)

518062-89-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 518062-89-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,1,8,0,6 and 2 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 518062-89:
(8*5)+(7*1)+(6*8)+(5*0)+(4*6)+(3*2)+(2*8)+(1*9)=150
150 % 10 = 0
So 518062-89-0 is a valid CAS Registry Number.

518062-89-0Downstream Products

518062-89-0Relevant articles and documents

6-Chloro-2(2H)-pyranone: A new 2(2H)-pyranone synthon

Biagetti, Matteo,Bellina, Fabio,Carpita, Adriano,Rossi, Renzo

, p. 607 - 610 (2007/10/03)

6-Chloro-2(2H)-pyranone, which can be prepared in high yield from commercially available trans-glutaconic acid, undergoes facile Pd/Cu-catalyzed reaction with various 1-alkynes to give rise to the corresponding 6-(1-alkynyl)-2(2H)-pyranones in moderate to good yields. These last hitherto unknown compounds have been used as direct precursors to 6-alkyl- and 6-[(Z)-1-alkenyl]-2(2H)-pyranones.

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