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1432725-79-5

(2-bromophenyl)(5,6-dimethoxyisoquinolin-1-yl)methanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1432725-79-5 Structure

  • Basic information

    1. Product Name: (2-bromophenyl)(5,6-dimethoxyisoquinolin-1-yl)methanone
    2. Synonyms: (2-bromophenyl)(5,6-dimethoxyisoquinolin-1-yl)methanone
    3. CAS NO:1432725-79-5
    4. Molecular Formula:
    5. Molecular Weight: 372.218
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1432725-79-5.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: (2-bromophenyl)(5,6-dimethoxyisoquinolin-1-yl)methanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2-bromophenyl)(5,6-dimethoxyisoquinolin-1-yl)methanone(1432725-79-5)
    11. EPA Substance Registry System: (2-bromophenyl)(5,6-dimethoxyisoquinolin-1-yl)methanone(1432725-79-5)

  • 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: 1432725-79-5(Hazardous Substances Data)

1432725-79-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1432725-79-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,3,2,7,2 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1432725-79:
(9*1)+(8*4)+(7*3)+(6*2)+(5*7)+(4*2)+(3*5)+(2*7)+(1*9)=155
155 % 10 = 5
So 1432725-79-5 is a valid CAS Registry Number.

1432725-79-5Downstream Products

1432725-79-5Relevant articles and documents

Direct conversion of 1-(2-bromobenzoyl)isoquinolines to dibenzo[ de,g ]quinolin-7-ones via reductive photocyclization

Chuang, Ta-Hsien,Li, Chien-Fu,Lee, Hong-Zin,Wen, Yu-Chia

, p. 4974 - 4984 (2013/06/27)

A series of A/D-ring substituted dibenzo[de,g]quinolin-7-ones was produced from the corresponding isoquinolinones and (2-bromophenyl)acetonitriles in four steps. This represents a convenient approach toward the synthesis of tetracyclic alkaloids. A direct conversion of 1-(2-bromobenzoyl)isoquinolines to dibenzo[de,g]quinolin-7-ones is the key step in the total synthesis. The yield of the reductive photocyclization depends on the position of the substituents at the isoquinolyl ring and the phenyl group. The mechanism of the reductive photocyclization is also discussed.

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