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CAS

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1395726-53-0

methyl 4-(4-methoxyphenyl)-3-[2-(4-methoxyphenyl)ethynyl]isoquinolin-7-yl ether is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1395726-53-0 Structure

  • Basic information

    1. Product Name: methyl 4-(4-methoxyphenyl)-3-[2-(4-methoxyphenyl)ethynyl]isoquinolin-7-yl ether
    2. Synonyms: methyl 4-(4-methoxyphenyl)-3-[2-(4-methoxyphenyl)ethynyl]isoquinolin-7-yl ether
    3. CAS NO:1395726-53-0
    4. Molecular Formula:
    5. Molecular Weight: 395.458
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1395726-53-0.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: methyl 4-(4-methoxyphenyl)-3-[2-(4-methoxyphenyl)ethynyl]isoquinolin-7-yl ether(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl 4-(4-methoxyphenyl)-3-[2-(4-methoxyphenyl)ethynyl]isoquinolin-7-yl ether(1395726-53-0)
    11. EPA Substance Registry System: methyl 4-(4-methoxyphenyl)-3-[2-(4-methoxyphenyl)ethynyl]isoquinolin-7-yl ether(1395726-53-0)

  • 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: 1395726-53-0(Hazardous Substances Data)

1395726-53-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1395726-53-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,5,7,2 and 6 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1395726-53:
(9*1)+(8*3)+(7*9)+(6*5)+(5*7)+(4*2)+(3*6)+(2*5)+(1*3)=200
200 % 10 = 0
So 1395726-53-0 is a valid CAS Registry Number.

1395726-53-0Relevant articles and documents

Synthesis of 8-aryl substituted benzo[a]phenanthridine derivatives by consecutive three component tandem reaction and 6-endo carbocyclization

Mandadapu, Anil K.,Dathi, Meena D.,Arigela, Rajesh K.,Kundu, Bijoy

experimental part, p. 8207 - 8215 (2012/09/22)

A concise construction of benzo[a]phenanthridines involving multicomponent tandem reaction/carbocyclization in a sequential format is described. The reaction proceeds initially via formation of a 4-aryl-3-arylethynyl-isoquinoline from 2-bromobenzaldehyde/tert-butylamine/1,3-diyne in a three component format followed by a second ring closure either via gold/silver catalyzed intramolecular hydroarylation or via iodo-catalyzed regioselective 6-endo-dig electrophilic cyclization. The salient feature of the strategy involves a three component reaction followed by transformation of the resulting product in to polyheterocycles with increased structural complexity in two steps.

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