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935280-14-1

5(4H)-Oxazolone, 4-(1-naphthalenyl)-2-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 935280-14-1 Structure

  • Basic information

    1. Product Name: 5(4H)-Oxazolone, 4-(1-naphthalenyl)-2-phenyl-
    2. Synonyms: 5(4H)-Oxazolone, 4-(1-naphthalenyl)-2-phenyl-
    3. CAS NO:935280-14-1
    4. Molecular Formula: C19H13NO2
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 935280-14-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 5(4H)-Oxazolone, 4-(1-naphthalenyl)-2-phenyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5(4H)-Oxazolone, 4-(1-naphthalenyl)-2-phenyl-(935280-14-1)
    11. EPA Substance Registry System: 5(4H)-Oxazolone, 4-(1-naphthalenyl)-2-phenyl-(935280-14-1)

  • 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: 935280-14-1(Hazardous Substances Data)

935280-14-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 935280-14-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,5,2,8 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 935280-14:
(8*9)+(7*3)+(6*5)+(5*2)+(4*8)+(3*0)+(2*1)+(1*4)=171
171 % 10 = 1
So 935280-14-1 is a valid CAS Registry Number.

935280-14-1Relevant articles and documents

Intermolecular ene reactions utilizing oxazolones and enol ethers

Fisk, Jason S.,Tepe, Jetze J.

, p. 3058 - 3059 (2007)

We report herein an intermolecular ene reaction using oxazolones with enol ethers which results in the formation of novel quaternary amino esters in near quantitative yields. The overall reaction transformation closely resembles an intermolecular version of the Conia-ene reaction. The reactions are uncatalyzed and occur under very mild conditions. Copyright

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