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1208004-07-2

N-(4-(N-(2-fluoropropyl)sulfamoyl)phenyl)-acetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1208004-07-2 Structure

  • Basic information

    1. Product Name: N-(4-(N-(2-fluoropropyl)sulfamoyl)phenyl)-acetamide
    2. Synonyms: N-(4-(N-(2-fluoropropyl)sulfamoyl)phenyl)-acetamide
    3. CAS NO:1208004-07-2
    4. Molecular Formula:
    5. Molecular Weight: 274.316
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1208004-07-2.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-(4-(N-(2-fluoropropyl)sulfamoyl)phenyl)-acetamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(4-(N-(2-fluoropropyl)sulfamoyl)phenyl)-acetamide(1208004-07-2)
    11. EPA Substance Registry System: N-(4-(N-(2-fluoropropyl)sulfamoyl)phenyl)-acetamide(1208004-07-2)

  • 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: 1208004-07-2(Hazardous Substances Data)

1208004-07-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1208004-07-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,8,0,0 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1208004-07:
(9*1)+(8*2)+(7*0)+(6*8)+(5*0)+(4*0)+(3*4)+(2*0)+(1*7)=92
92 % 10 = 2
So 1208004-07-2 is a valid CAS Registry Number.

1208004-07-2Downstream Products

1208004-07-2Relevant articles and documents

Carbonic Anhydrases inhibitory effects of new benzenesulfonamides synthesized by using superacid chemistry

Liu, Fei,Martin-Mingot, Agnès,Lecornué,Jouannetaud, Marie-Paule,Maresca, Alfonso,Thibaudeau, Sebastien,Supuran, Claudiu T.

, p. 886 - 891 (2013/02/23)

A series of benzofused sultams and fluorinated benzenesulfonamides were synthesized in superacid HF/SbF5 from simple N-allylic derivatives. Almost all of these original compounds showed micromolar inhibitory activities against carbonic anhydrases I and II

Superelectrophilic activation in superacid HF/SbF5 and synthesis of benzofused sultams

Liu, Fei,Martin-Mingot, Agnes,Jouannetaud, Marie-Paule,Zunino, Fabien,Thibaudeau, Sebastien

supporting information; experimental part, p. 868 - 871 (2010/04/27)

(Figure Presented) The synthesis of benzofused sultams and/or fluorlnated sulfonamides, starting from N-allyllc sulfonamides, was performed In superacid HF/ SbF5, through superelectrophilic activation. A dramatic effect of superacid composition on the selectivity of the reaction was shown and applied to the synthesis of cyclic 4-aminobenzenesulfonamides.

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