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1314593-71-9

C28H23BrN2O2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1314593-71-9 Structure

  • Basic information

    1. Product Name: C28H23BrN2O2
    2. Synonyms:
    3. CAS NO:1314593-71-9
    4. Molecular Formula:
    5. Molecular Weight: 499.407
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1314593-71-9.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: C28H23BrN2O2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C28H23BrN2O2(1314593-71-9)
    11. EPA Substance Registry System: C28H23BrN2O2(1314593-71-9)

  • 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: 1314593-71-9(Hazardous Substances Data)

1314593-71-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1314593-71-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,4,5,9 and 3 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1314593-71:
(9*1)+(8*3)+(7*1)+(6*4)+(5*5)+(4*9)+(3*3)+(2*7)+(1*1)=149
149 % 10 = 9
So 1314593-71-9 is a valid CAS Registry Number.

1314593-71-9Downstream Products

1314593-71-9Relevant articles and documents

Synthesis of 5-acetyloxazoles and 1,2-diketones from β-alkoxy-β- ketoenamides and their subsequent transformations

Lechel, Tilman,Gerhard, Markus,Trawny, Daniel,Brusilowskij, Boris,Schefzig, Luise,Zimmer, Reinhold,Rabe, Juergen P.,Lentz, Dieter,Schalley, Christoph A.,Reissig, Hans-Ulrich

experimental part, p. 7480 - 7491 (2011/08/08)

Lithiated alkoxyallenes, nitriles, and carboxylic acids have been employed as precursors in a three-component reaction leading to highly substituted β-alkoxy-β-ketoenamides. Upon treatment with trifluoroacetic acid, these enamides could be easily cyclized

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