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  • 872579-13-0 Structure
  • Basic information

    1. Product Name: C41H47N2O12
    2. Synonyms: C41H47N2O12
    3. CAS NO:872579-13-0
    4. Molecular Formula:
    5. Molecular Weight: 759.83
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 872579-13-0.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: C41H47N2O12(CAS DataBase Reference)
    10. NIST Chemistry Reference: C41H47N2O12(872579-13-0)
    11. EPA Substance Registry System: C41H47N2O12(872579-13-0)
  • 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: 872579-13-0(Hazardous Substances Data)

872579-13-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 872579-13-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,2,5,7 and 9 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 872579-13:
(8*8)+(7*7)+(6*2)+(5*5)+(4*7)+(3*9)+(2*1)+(1*3)=210
210 % 10 = 0
So 872579-13-0 is a valid CAS Registry Number.

872579-13-0Downstream Products

872579-13-0Relevant articles and documents

Synthesis of novel spin-labeled derivatives of podophyllotoxin as potential antineoplastic agents

Liu, Ying-Qian,Tian, Xuan

, p. 2749 - 2758 (2005)

Five novel nitroxyl spin-labeled ester derivatives of podophyllotoxin have been prepared by reacting the corresponding N-(1-oxyl-2,2,6,6-tetramethyl-4- piperidinyloxy-carbonyl) amino acids with the hydroxy group of podophyllotoxin in the presence of dimethylaminopyridine and N,N-dicyclohexylcarbodiimide and evaluated as potential antitumor agents. All of the target compounds showed more significant cytotoxicity against P-388 murine leukemia and A-549 human lung carcinoma in vitro than etoposide. Copyright Taylor & Francis, Inc.

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