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1440513-09-6

C14H14N2O2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1440513-09-6 Structure

  • Basic information

    1. Product Name: C14H14N2O2
    2. Synonyms:
    3. CAS NO:1440513-09-6
    4. Molecular Formula:
    5. Molecular Weight: 242.277
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1440513-09-6.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: C14H14N2O2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C14H14N2O2(1440513-09-6)
    11. EPA Substance Registry System: C14H14N2O2(1440513-09-6)

  • 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: 1440513-09-6(Hazardous Substances Data)

1440513-09-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1440513-09-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,0,5,1 and 3 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1440513-09:
(9*1)+(8*4)+(7*4)+(6*0)+(5*5)+(4*1)+(3*3)+(2*0)+(1*9)=116
116 % 10 = 6
So 1440513-09-6 is a valid CAS Registry Number.

1440513-09-6Relevant articles and documents

NCN palladium pincer via transmercuration. Synthesis of [2-(2-oxazoliny)-6-(2-pyridyl)] phenylpalladium(II) chloride and its catalytic activity in Suzuki coupling

Li, Ping,Zhou, Hai-Feng,Liu, Fang,Hu, Zhao-Xia,Wang, Hong-Xing

, p. 78 - 81 (2013)

The unsymmetrical NCN ligand 1-(2-oxazolinyl)-3-(2-pyridyl)benzene 6 was synthesized starting from m-bromotoluene after a series of transformations. The reaction of 6 and mercury (II) acetate resulted in mercurial derivative 7 which was transformed into the corresponding NCN palladium pincer 8 via transmercuration. The ultraviolet spectra of 6-8 in acetonitrile were also studied. The structures of 6 and 8 were further confirmed by X-ray single crystal diffraction. The carbon-carbon cross coupling reactions between aryl halides and phenylboronic acid catalyzed by 8 were investigated. The results indicate that this palladium pincer is more highly active to the coupling of aryl bromides than aryl chlorides.

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