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[Ni(2-hydroxy-1-naphthaldehyde thiosemicarbazone)(triphenylphosphine)]Cl*H2O is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1417424-10-2 Structure
  • Basic information

    1. Product Name: [Ni(2-hydroxy-1-naphthaldehyde thiosemicarbazone)(triphenylphosphine)]Cl*H2O
    2. Synonyms:
    3. CAS NO:1417424-10-2
    4. Molecular Formula:
    5. Molecular Weight: 618.746
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1417424-10-2.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: [Ni(2-hydroxy-1-naphthaldehyde thiosemicarbazone)(triphenylphosphine)]Cl*H2O(CAS DataBase Reference)
    10. NIST Chemistry Reference: [Ni(2-hydroxy-1-naphthaldehyde thiosemicarbazone)(triphenylphosphine)]Cl*H2O(1417424-10-2)
    11. EPA Substance Registry System: [Ni(2-hydroxy-1-naphthaldehyde thiosemicarbazone)(triphenylphosphine)]Cl*H2O(1417424-10-2)
  • 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: 1417424-10-2(Hazardous Substances Data)

1417424-10-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1417424-10-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,7,4,2 and 4 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1417424-10:
(9*1)+(8*4)+(7*1)+(6*7)+(5*4)+(4*2)+(3*4)+(2*1)+(1*0)=132
132 % 10 = 2
So 1417424-10-2 is a valid CAS Registry Number.

1417424-10-2Downstream Products

1417424-10-2Relevant articles and documents

DNA binding, antioxidant, cytotoxicity (MTT, lactate dehydrogenase, NO), and cellular uptake studies of structurally different nickel(II) thiosemicarbazone complexes: Synthesis, spectroscopy, electrochemistry, and X-ray crystallography

Prabhakaran,Kalaivani,Huang,Poornima,Vijaya Padma,Dallemer,Natarajan

, p. 233 - 247 (2013)

Three new nickel(II) thiosemicarbazone complexes have been synthesized and characterized by analytical, spectral, and single-crystal X-ray diffraction studies. In complex 1, the ligand 2-hydroxy-1-naphthaldehydethiosemicarbazone coordinated as a monobasic tridentate donor, whereas in complexes 2 and 3, the ligands salicylaldehyde-4(N)-ethylthiosemicarbazone and 2-hydroxy-1- naphthaldehyde-4(N)-ethylthiosemicarbazone coordinated as a dibasic tridentate donor. The DNA binding ability of the complexes in calf thymus DNA was explored by absorption and emission titration experiments. The antioxidant property of the new complexes was evaluated to test their free-radical scavenging ability. In vitro cytotoxicity assays were performed for the new complexes in A549 and HepG2 cell lines. The new compounds overcome cisplatin resistance in the A549 cell line and they were also active in the HepG2 cell line. The cellular uptake study showed the accumulation of the complexes in tumor cells depended on the nature of the ligand attached to the nickel ion. Graphical abstract: Structurally different nickel(II) thiosemicarbazone complexes for which DNA binding, antioxidant, cytotoxicity, and cellular uptake studies were performed [Figure not available: see fulltext.]

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