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CAS

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392304-81-3

(4-methoxyphenyl)(4-phenyl-3-quinolinyl)methanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 392304-81-3 Structure

  • Basic information

    1. Product Name: (4-methoxyphenyl)(4-phenyl-3-quinolinyl)methanone
    2. Synonyms: (4-methoxyphenyl)(4-phenyl-3-quinolinyl)methanone
    3. CAS NO:392304-81-3
    4. Molecular Formula: C23H17NO2
    5. Molecular Weight: 339.38658
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 392304-81-3.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: (4-methoxyphenyl)(4-phenyl-3-quinolinyl)methanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: (4-methoxyphenyl)(4-phenyl-3-quinolinyl)methanone(392304-81-3)
    11. EPA Substance Registry System: (4-methoxyphenyl)(4-phenyl-3-quinolinyl)methanone(392304-81-3)

  • 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: 392304-81-3(Hazardous Substances Data)

392304-81-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 392304-81-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,9,2,3,0 and 4 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 392304-81:
(8*3)+(7*9)+(6*2)+(5*3)+(4*0)+(3*4)+(2*8)+(1*1)=143
143 % 10 = 3
So 392304-81-3 is a valid CAS Registry Number.

392304-81-3Downstream Products

392304-81-3Relevant articles and documents

Chemoselective Synthesis of N -Arylenaminones and 3-Aroylquinolines by Synergistic Control of Temperature and Amount of Catalyst

Zhou, Pan,Hu, Biao,Rao, Kairui,Li, Lingdan,Yang, Jiao,Gao, Chuanzhu,Wang, Fengping,Yu, Fuchao

supporting information, p. 519 - 524 (2017/11/29)

An efficient and practical method has been developed for the divergent synthesis of N -arylenaminones and 3-aroylquinolines from 2-aminoaryl ketones and N, N -dimethylenaminones in the presence of 4-toluenesulfonic acid through synergistic control of the

ZnCl2-promoted Friedl?nder-type synthesis of 4-substituted 3-aroyl quinolines from o-aminoaryl ketones and enaminones

Luo, Laichun,Zhou, Zongbao,Zhu, Jiayi,Lu, Xue,Wang, Hong

supporting information, p. 4987 - 4990 (2016/10/21)

A practical synthesis of 4-substituted 3-aroyl quinolines via Friedl?nder-type reaction from readily available o-aminoaryl ketones and enaminones was developed. In the presence of ZnCl2, the reaction proceeded smoothly affording the desired products with various functional groups in moderate to good yields.

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