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351363-07-0

C18H20N2O2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 351363-07-0 Structure

  • Basic information

    1. Product Name: C18H20N2O2
    2. Synonyms: C18H20N2O2
    3. CAS NO:351363-07-0
    4. Molecular Formula:
    5. Molecular Weight: 296.369
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 351363-07-0.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: C18H20N2O2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C18H20N2O2(351363-07-0)
    11. EPA Substance Registry System: C18H20N2O2(351363-07-0)

  • 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: 351363-07-0(Hazardous Substances Data)

351363-07-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 351363-07-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,1,3,6 and 3 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 351363-07:
(8*3)+(7*5)+(6*1)+(5*3)+(4*6)+(3*3)+(2*0)+(1*7)=120
120 % 10 = 0
So 351363-07-0 is a valid CAS Registry Number.

351363-07-0Relevant articles and documents

Cu(II) catalyzed imine C-H functionalization leading to synthesis of 2,5-substituted 1,3,4-oxadiazoles

Guin, Srimanta,Ghosh, Tuhin,Rout, Saroj Kumar,Banerjee, Arghya,Patel, Bhisma K.

, p. 5976 - 5979 (2011)

A direct access to symmetrical and unsymmetrical 2,5-disubstituted [1,3,4]-oxadiazoles has been accomplished through an imine C-H functionalization of N-arylidenearoylhydrazide using a catalytic quantity of Cu(OTf)2. This is the first example of amidic oxygen functioning as a nucleophile in a Cu-catalyzed oxidative coupling of an imine C-H bond. These reactions can be performed in air atmosphere and moisture making it exceptionally practical for application in organic synthesis.

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