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425613-39-4

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

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  • 425613-39-4 Structure

  • Basic information

    1. Product Name: N-(3,4-dimethoxyphenyl)methanesulfonamide
    2. Synonyms: N-(3,4-dimethoxyphenyl)methanesulfonamide
    3. CAS NO:425613-39-4
    4. Molecular Formula: C9H13NO4S
    5. Molecular Weight: 231.26882
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 425613-39-4.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: N-(3,4-dimethoxyphenyl)methanesulfonamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(3,4-dimethoxyphenyl)methanesulfonamide(425613-39-4)
    11. EPA Substance Registry System: N-(3,4-dimethoxyphenyl)methanesulfonamide(425613-39-4)

  • 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: 425613-39-4(Hazardous Substances Data)

425613-39-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 425613-39-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,2,5,6,1 and 3 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 425613-39:
(8*4)+(7*2)+(6*5)+(5*6)+(4*1)+(3*3)+(2*3)+(1*9)=134
134 % 10 = 4
So 425613-39-4 is a valid CAS Registry Number.

425613-39-4Downstream Products

425613-39-4Relevant articles and documents

A practical route to quinolines from anilines

Tokuyama, Hidetoshi,Sato, Masashi,Ueda, Toshihiro,Fukuyama, Tohru

, p. 105 - 108 (2007/10/03)

A practical route to quinoline from anilines through acid-mediated cyclization of 3-(N-aryl-N-sulfonylamino)propionaldehydes has been developed. Treatment of the cyclization products, dihydroquinoline intermediates with KOH in DMSO leads to substituted quinolines.

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