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1428369-91-8

C15H14N6O2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1428369-91-8 Structure

  • Basic information

    1. Product Name: C15H14N6O2
    2. Synonyms: C15H14N6O2
    3. CAS NO:1428369-91-8
    4. Molecular Formula:
    5. Molecular Weight: 310.315
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1428369-91-8.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: C15H14N6O2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C15H14N6O2(1428369-91-8)
    11. EPA Substance Registry System: C15H14N6O2(1428369-91-8)

  • 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: 1428369-91-8(Hazardous Substances Data)

1428369-91-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1428369-91-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,8,3,6 and 9 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1428369-91:
(9*1)+(8*4)+(7*2)+(6*8)+(5*3)+(4*6)+(3*9)+(2*9)+(1*1)=188
188 % 10 = 8
So 1428369-91-8 is a valid CAS Registry Number.

1428369-91-8Downstream Products

1428369-91-8Relevant articles and documents

Novel 1-acyl-4-substituted semicarbazide derivatives of primaquine-synthesis, cytostatic, antiviral and antioxidative studies

Perkovic, Ivana,Trsinar, Sara,Zanetic, Jelena,Kralj, Marijeta,Martin-Kleiner, Irena,Balzarini, Jan,Hadjipavlou-Litina, Dimitra,Katsori, Anna Maria,Zorc, Branka

, p. 601 - 610 (2013/05/22)

A series of novel 1,4-substituted semicarbazides 5a-g with a primaquine moiety bridged by a carbonyl group at position 1 and a cycloalkyl, aryl, benzyloxy or hydroxy substituent at position 4 were prepared and biologically evaluated. The synthetic pathway

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