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  • 1391724-39-2 Structure
  • Basic information

    1. Product Name: C67H52N6O9Zn
    2. Synonyms: C67H52N6O9Zn
    3. CAS NO:1391724-39-2
    4. Molecular Formula:
    5. Molecular Weight: 1150.57
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1391724-39-2.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: C67H52N6O9Zn(CAS DataBase Reference)
    10. NIST Chemistry Reference: C67H52N6O9Zn(1391724-39-2)
    11. EPA Substance Registry System: C67H52N6O9Zn(1391724-39-2)
  • 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: 1391724-39-2(Hazardous Substances Data)

1391724-39-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1391724-39-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,1,7,2 and 4 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1391724-39:
(9*1)+(8*3)+(7*9)+(6*1)+(5*7)+(4*2)+(3*4)+(2*3)+(1*9)=172
172 % 10 = 2
So 1391724-39-2 is a valid CAS Registry Number.

1391724-39-2Upstream product

1391724-39-2Downstream Products

1391724-39-2Relevant articles and documents

Comparative studies of the cellular uptake, subcellular localization, and cytotoxic and phototoxic antitumor properties of ruthenium(II)-porphyrin conjugates with different linkers

Zhang, Jing-Xiang,Zhou, Jun-Wei,Chan, Chi-Fai,Lau, Terrence Chi-Kong,Kwong, Daniel W. J.,Tam, Hoi-Lam,Mak, Nai-Ki,Wong, Ka-Leung,Wong, Wai-Kwok

, p. 1623 - 1638 (2012)

Six water-soluble free-base porphyrin-Ru(II) conjugates, 1-3, and Zn(II) porphyrin-Ru(II) conjugates, 4-6, with different linkers between the hydrophobic porphyrin moiety and the hydrophilic Ru(II)-polypyridyl complex, have been synthesized. The linear and two-photon-induced photophysical properties of these conjugates were measured and evaluated for their potential application as dual in vitro imaging and photodynamic therapeutic (PDT) agents. Conjugates 1-3, with their high luminescence and singlet oxygen quantum yields, were selected for further study of their cellular uptake, subcellular localization, and cytotoxic and photocytotoxic (under linear and two-photon excitation) properties using HeLa cells. Conjugate 2, with its hydrophobic phenylethynyl linker, was shown to be highly promising for further development as a bifunctional probe for two-photon (NIR) induced PDT and in vitro imaging. Cellular uptake and subcellular localization properties were shown to be crucial to its PDT efficacy.

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