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1217794-38-1

C23H20ClF2N7O5 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1217794-38-1 Structure

  • Basic information

    1. Product Name: C23H20ClF2N7O5
    2. Synonyms:
    3. CAS NO:1217794-38-1
    4. Molecular Formula:
    5. Molecular Weight: 547.906
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1217794-38-1.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: C23H20ClF2N7O5(CAS DataBase Reference)
    10. NIST Chemistry Reference: C23H20ClF2N7O5(1217794-38-1)
    11. EPA Substance Registry System: C23H20ClF2N7O5(1217794-38-1)

  • 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: 1217794-38-1(Hazardous Substances Data)

1217794-38-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1217794-38-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,7,7,9 and 4 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1217794-38:
(9*1)+(8*2)+(7*1)+(6*7)+(5*7)+(4*9)+(3*4)+(2*3)+(1*8)=171
171 % 10 = 1
So 1217794-38-1 is a valid CAS Registry Number.

1217794-38-1Downstream Products

1217794-38-1Relevant articles and documents

Novel small molecule bradykinin B1 receptor antagonists. Part 1: Benzamides and semicarbazides

Schaudt, Marco,Locardi, Elsa,Zischinsky, Gunther,Stragies, Roland,Pfeifer, Jochen R.,Gibson, Christoph,Scharn, Dirk,Richter, Uwe,Kalkhof, Holger,Dinkel, Klaus,Schnatbaum, Karsten

scheme or table, p. 1225 - 1228 (2010/06/15)

The synthesis and SAR of two series of bradykinin B1 receptor antagonists is described. The benzamide moiety proved to be a suitable replacement for the aryl ester functionality of biaryl based antagonists. In addition, it was found that semica

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