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1310366-71-2

N-acetyloxy-2-bromobenzenesulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1310366-71-2 Structure

  • Basic information

    1. Product Name: N-acetyloxy-2-bromobenzenesulfonamide
    2. Synonyms: N-acetyloxy-2-bromobenzenesulfonamide
    3. CAS NO:1310366-71-2
    4. Molecular Formula:
    5. Molecular Weight: 294.126
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1310366-71-2.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-acetyloxy-2-bromobenzenesulfonamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-acetyloxy-2-bromobenzenesulfonamide(1310366-71-2)
    11. EPA Substance Registry System: N-acetyloxy-2-bromobenzenesulfonamide(1310366-71-2)

  • 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: 1310366-71-2(Hazardous Substances Data)

1310366-71-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1310366-71-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,0,3,6 and 6 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1310366-71:
(9*1)+(8*3)+(7*1)+(6*0)+(5*3)+(4*6)+(3*6)+(2*7)+(1*1)=112
112 % 10 = 2
So 1310366-71-2 is a valid CAS Registry Number.

1310366-71-2Relevant articles and documents

Optimization of HNO production from N, O - Bis -acylated hydroxylamine derivatives

Sutton, Art D.,Williamson, Morgan,Weismiller, Hilary,Toscano, John P.

, p. 472 - 475 (2012/03/26)

A wide range of N,O-bis-acylated hydroxylamine derivatives with chloro or arenesulfonyl leaving groups, and a related set of N-hydroxy-N-acylsulfonamides, have been synthesized and evaluated for nitroxyl (HNO) production. Mechanistic studies have revealed that the observed aqueous chemistry is more complicated than originally anticipated, and have been used to develop a new series of efficient HNO precursors (4u-4x, 7c-7d) with tunable half-lives.

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