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1398743-14-0

N-tert-butyl-2-phenylquinoline-3-carboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1398743-14-0 Structure

  • Basic information

    1. Product Name: N-tert-butyl-2-phenylquinoline-3-carboxamide
    2. Synonyms: N-tert-butyl-2-phenylquinoline-3-carboxamide
    3. CAS NO:1398743-14-0
    4. Molecular Formula:
    5. Molecular Weight: 304.392
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1398743-14-0.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: N-tert-butyl-2-phenylquinoline-3-carboxamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-tert-butyl-2-phenylquinoline-3-carboxamide(1398743-14-0)
    11. EPA Substance Registry System: N-tert-butyl-2-phenylquinoline-3-carboxamide(1398743-14-0)

  • 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: 1398743-14-0(Hazardous Substances Data)

1398743-14-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1398743-14-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,8,7,4 and 3 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1398743-14:
(9*1)+(8*3)+(7*9)+(6*8)+(5*7)+(4*4)+(3*3)+(2*1)+(1*4)=210
210 % 10 = 0
So 1398743-14-0 is a valid CAS Registry Number.

1398743-14-0Downstream Products

1398743-14-0Relevant articles and documents

Palladium-catalyzed sequential formation of C-C bonds: Efficient assembly of 2-substituted and 2,3-disubstituted quinolines

Ji, Xiaochen,Huang, Huawen,Li, Yibiao,Chen, Huoji,Jiang, Huanfeng

, p. 7292 - 7296 (2012)

A series of substituted quinolines was prepared from arylamines, aldehydes, and terminal olefins (see scheme). The palladium-catalyzed sequential formation of C-C bonds proceeds smoothly with both electron-deficient and electron-rich olefins. When acrylic acid is used as terminal olefin, decarboxylation occurs to provide 2-substituted quinolines. Copyright

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