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  • 1228305-09-6 Structure
  • Basic information

    1. Product Name: C14H19NO3
    2. Synonyms:
    3. CAS NO:1228305-09-6
    4. Molecular Formula:
    5. Molecular Weight: 249.31
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1228305-09-6.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: C14H19NO3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C14H19NO3(1228305-09-6)
    11. EPA Substance Registry System: C14H19NO3(1228305-09-6)
  • 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: 1228305-09-6(Hazardous Substances Data)

1228305-09-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1228305-09-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,8,3,0 and 5 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1228305-09:
(9*1)+(8*2)+(7*2)+(6*8)+(5*3)+(4*0)+(3*5)+(2*0)+(1*9)=126
126 % 10 = 6
So 1228305-09-6 is a valid CAS Registry Number.

1228305-09-6Downstream Products

1228305-09-6Relevant articles and documents

Discovery of triarylethanolamine inhibitors of the Kv1.5 potassium channel

Beshore, Douglas C.,Liverton, Nigel J.,McIntyre, Charles J.,Claiborne, Christopher F.,Libby, Brian,Culberson, J. Christopher,Salata, Joseph J.,Regan, Christopher P.,Lynch, Joseph J.,Kiss, Laszlo,Spencer, Robert H.,Kane, Stephanie A.,White, Rebecca B.,Yeh, Suzie,Hartman, George D.,Dinsmore, Christopher J.

scheme or table, p. 2493 - 2496 (2010/08/06)

A series of triarylethanolamine inhibitors of the Kv1.5 potassium channel have been prepared and evaluated for their effects in vitro and in vivo. The structure-activity relationship (SAR) studies described herein led to the development of potent, selecti

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