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136138-34-6

N-(2-Fluoro-6-methoxy-benzoyl)-N-(2-iodo-phenyl)-4-methyl-benzenesulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 136138-34-6 Structure

  • Basic information

    1. Product Name: N-(2-Fluoro-6-methoxy-benzoyl)-N-(2-iodo-phenyl)-4-methyl-benzenesulfonamide
    2. Synonyms: N-(2-Fluoro-6-methoxy-benzoyl)-N-(2-iodo-phenyl)-4-methyl-benzenesulfonamide
    3. CAS NO:136138-34-6
    4. Molecular Formula:
    5. Molecular Weight: 525.339
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 136138-34-6.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: N-(2-Fluoro-6-methoxy-benzoyl)-N-(2-iodo-phenyl)-4-methyl-benzenesulfonamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(2-Fluoro-6-methoxy-benzoyl)-N-(2-iodo-phenyl)-4-methyl-benzenesulfonamide(136138-34-6)
    11. EPA Substance Registry System: N-(2-Fluoro-6-methoxy-benzoyl)-N-(2-iodo-phenyl)-4-methyl-benzenesulfonamide(136138-34-6)

  • 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: 136138-34-6(Hazardous Substances Data)

136138-34-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 136138-34-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,1,3 and 8 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 136138-34:
(8*1)+(7*3)+(6*6)+(5*1)+(4*3)+(3*8)+(2*3)+(1*4)=116
116 % 10 = 6
So 136138-34-6 is a valid CAS Registry Number.

136138-34-6Relevant articles and documents

A Short Efficient Route to Acronycine and Other Acridones

Horne, Stephen,Rodrigo, Russell

, p. 1046 - 1048 (1991)

A Fries type rearrangement of N-tosyl-o-iodobenzanilides, triggered by lithium-iodine exchange at low temperature is the key step in a general, regiospecific synthesis of acridones.

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