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

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  • 1310366-00-7 Structure
  • Basic information

    1. Product Name: N-(2-bromobenzenesulfonyl)-N-acetyloxy-acetamide
    2. Synonyms: N-(2-bromobenzenesulfonyl)-N-acetyloxy-acetamide
    3. CAS NO:1310366-00-7
    4. Molecular Formula:
    5. Molecular Weight: 336.163
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1310366-00-7.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-bromobenzenesulfonyl)-N-acetyloxy-acetamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(2-bromobenzenesulfonyl)-N-acetyloxy-acetamide(1310366-00-7)
    11. EPA Substance Registry System: N-(2-bromobenzenesulfonyl)-N-acetyloxy-acetamide(1310366-00-7)
  • 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: 1310366-00-7(Hazardous Substances Data)

1310366-00-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1310366-00-7 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, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1310366-00:
(9*1)+(8*3)+(7*1)+(6*0)+(5*3)+(4*6)+(3*6)+(2*0)+(1*0)=97
97 % 10 = 7
So 1310366-00-7 is a valid CAS Registry Number.

1310366-00-7Relevant 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.

Bis-Acylated Hydroxylamine Derivatives

-

Page/Page column 36, (2011/06/24)

The invention provides certain bis-acylated hydroxylamine derivative compounds, pharmaceutical compositions and kits comprising such compounds, and methods of using such compounds or pharmaceutical compositions. In particular, the invention provides methods of using such compounds or pharmaceutical compositions for treating, preventing, or delaying the onset and/or develop of a disease or condition. In some embodiments, the disease or condition is selected from cardiovascular diseases, ischemia, reperfusion injury, cancerous disease, pulmonary hypertension and conditions responsive to nitroxyl therapy.

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