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1428340-05-9

C13H15N3O is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1428340-05-9 Structure

  • Basic information

    1. Product Name: C13H15N3O
    2. Synonyms: C13H15N3O
    3. CAS NO:1428340-05-9
    4. Molecular Formula:
    5. Molecular Weight: 229.282
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1428340-05-9.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: C13H15N3O(CAS DataBase Reference)
    10. NIST Chemistry Reference: C13H15N3O(1428340-05-9)
    11. EPA Substance Registry System: C13H15N3O(1428340-05-9)

  • 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: 1428340-05-9(Hazardous Substances Data)

1428340-05-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1428340-05-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,8,3,4 and 0 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1428340-05:
(9*1)+(8*4)+(7*2)+(6*8)+(5*3)+(4*4)+(3*0)+(2*0)+(1*5)=139
139 % 10 = 9
So 1428340-05-9 is a valid CAS Registry Number.

1428340-05-9Downstream Products

1428340-05-9Relevant articles and documents

Design, synthesis, and molecular modelling of pyridazinone and phthalazinone derivatives as protein kinases inhibitors

Elagawany, Mohamed,Ibrahim, Mohamed A.,Ali Ahmed, Hany Emary,El-Etrawy, A.Sh.,Ghiaty, Adel,Abdel-Samii, Zakaria K.,El-Feky, Said A.,Bajorath, Juergen

supporting information, p. 2007 - 2013 (2013/05/09)

The design and synthesis of pyridazinone and phthalazinone derivatives are described. Newly synthesized compounds were tested on a panel of four kinases in order to evaluate their activity and potential selectivity. In addition, the promising compounds were tested on four cancer cell lines to examine cytotoxic effects. The compounds inhibited DYRK1A and GSK3 with different activity. SAR analysis and docking calculations were carried out to aid in the interpretation of the results. Taken together, our findings suggest that pyridazinone and phthalazinone scaffolds are interesting starting points for design of potent GSK3 and DYRK1A inhibitors.

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