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1338246-27-7

1,5-bis(3,4-dimethoxyphenyl)anthracene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1338246-27-7 Structure

  • Basic information

    1. Product Name: 1,5-bis(3,4-dimethoxyphenyl)anthracene
    2. Synonyms: 1,5-bis(3,4-dimethoxyphenyl)anthracene
    3. CAS NO:1338246-27-7
    4. Molecular Formula:
    5. Molecular Weight: 450.534
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1338246-27-7.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: 1,5-bis(3,4-dimethoxyphenyl)anthracene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,5-bis(3,4-dimethoxyphenyl)anthracene(1338246-27-7)
    11. EPA Substance Registry System: 1,5-bis(3,4-dimethoxyphenyl)anthracene(1338246-27-7)

  • 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: 1338246-27-7(Hazardous Substances Data)

1338246-27-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1338246-27-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,8,2,4 and 6 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1338246-27:
(9*1)+(8*3)+(7*3)+(6*8)+(5*2)+(4*4)+(3*6)+(2*2)+(1*7)=157
157 % 10 = 7
So 1338246-27-7 is a valid CAS Registry Number.

1338246-27-7Relevant articles and documents

Synthesis of 1,5-substituted anthracenes by means of Kumada coupling and their derivatization

Bringmann, Sebastian,Ahmed, Saleh A.,Hartmann, Ramona,Mattay, Jochen

, p. 2291 - 2296 (2011)

Herein, we present a method to access a series of 1,5-functionalized anthracenes through Kumada coupling. All syntheses start from readily available 1,5-dichloroanthracene. The so-formed anthracenes are further derivatized to enable, for example, attachme

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