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CAS

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1337563-02-6

6-(3-methoxybenzene)isoquinoline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1337563-02-6 Structure

  • Basic information

    1. Product Name: 6-(3-methoxybenzene)isoquinoline
    2. Synonyms: 6-(3-methoxybenzene)isoquinoline
    3. CAS NO:1337563-02-6
    4. Molecular Formula:
    5. Molecular Weight: 235.285
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1337563-02-6.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: 6-(3-methoxybenzene)isoquinoline(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-(3-methoxybenzene)isoquinoline(1337563-02-6)
    11. EPA Substance Registry System: 6-(3-methoxybenzene)isoquinoline(1337563-02-6)

  • 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: 1337563-02-6(Hazardous Substances Data)

1337563-02-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1337563-02-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,7,5,6 and 3 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1337563-02:
(9*1)+(8*3)+(7*3)+(6*7)+(5*5)+(4*6)+(3*3)+(2*0)+(1*2)=156
156 % 10 = 6
So 1337563-02-6 is a valid CAS Registry Number.

1337563-02-6Downstream Products

1337563-02-6Relevant articles and documents

Palladium-catalyzed Hiyama cross-coupling of aryltrifluorosilanes with aryl and heteroaryl chlorides

Molander, Gary A.,Iannazzo, Laura

, p. 9182 - 9187 (2011/12/16)

An efficient, palladium-catalyzed Hiyama cross-coupling reaction of aryltrifluorosilanes with aryl chlorides has been developed. A wide variety of functionalized biaryl derivatives were isolated in good to excellent yields. The scope of this reaction has also been extended to heteroaryl chlorides, affording the corresponding heterobiaryl compounds in high yields.

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