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1310552-60-3

N-amino(phenyl)methylene-2,5-dibromo-1-benzenesulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1310552-60-3 Structure

  • Basic information

    1. Product Name: N-amino(phenyl)methylene-2,5-dibromo-1-benzenesulfonamide
    2. Synonyms: N-amino(phenyl)methylene-2,5-dibromo-1-benzenesulfonamide
    3. CAS NO:1310552-60-3
    4. Molecular Formula:
    5. Molecular Weight: 418.109
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1310552-60-3.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-amino(phenyl)methylene-2,5-dibromo-1-benzenesulfonamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-amino(phenyl)methylene-2,5-dibromo-1-benzenesulfonamide(1310552-60-3)
    11. EPA Substance Registry System: N-amino(phenyl)methylene-2,5-dibromo-1-benzenesulfonamide(1310552-60-3)

  • 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: 1310552-60-3(Hazardous Substances Data)

1310552-60-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1310552-60-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,0,5,5 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1310552-60:
(9*1)+(8*3)+(7*1)+(6*0)+(5*5)+(4*5)+(3*2)+(2*6)+(1*0)=103
103 % 10 = 3
So 1310552-60-3 is a valid CAS Registry Number.

1310552-60-3Relevant articles and documents

Facile synthesis of 4H-1,2,4-benzothiadiazine-1,1-dioxides

Cherepakha, Artem,Kovtunenko, Vladimir O.,Tolmachev, Andrey,Lukin, Oleg,Nazarenko, Konstantin G.

, p. 1977 - 1989 (2011)

o-Bromoarylsulfonylated amidines prepared either by acylation of amidine with o-bromoarylsulfonyl chloride or through the reaction of o-bromoarylsulfoamide with lactime ether underwent Cu(I)-catalyzed intramolecular cyclization to give 4H-1,2,4-benzothiadiazine-1,1-dioxides in good yield. By varying substituents on arylsulfonyl moieties, amidines, and lactime ethers, a small library of structurally diverse 4H-1,2,4- benzothiadiazine-1,1-dioxide derivatives was prepared.

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