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C22H15BrN10OS2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1094597-78-0 Structure
  • Basic information

    1. Product Name: C22H15BrN10OS2
    2. Synonyms: C22H15BrN10OS2
    3. CAS NO:1094597-78-0
    4. Molecular Formula:
    5. Molecular Weight: 579.464
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1094597-78-0.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: C22H15BrN10OS2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C22H15BrN10OS2(1094597-78-0)
    11. EPA Substance Registry System: C22H15BrN10OS2(1094597-78-0)
  • 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: 1094597-78-0(Hazardous Substances Data)

1094597-78-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1094597-78-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,4,5,9 and 7 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1094597-78:
(9*1)+(8*0)+(7*9)+(6*4)+(5*5)+(4*9)+(3*7)+(2*7)+(1*8)=200
200 % 10 = 0
So 1094597-78-0 is a valid CAS Registry Number.

1094597-78-0Downstream Products

1094597-78-0Relevant articles and documents

Synthesis, biological and computational study of new Schiff base hydrazones bearing 3-(4-pyridine)-5-mercapto-1,2,4-triazole moiety

Khanmohammadi, Hamid,Abnosi, Mohammad H.,Hosseinzadeh, Ali,Erfantalab, Malihe

experimental part, p. 1474 - 1480 (2009/02/06)

A series of new Schiff base hydrazones (compounds 1-16) were synthesized by condensation reaction of 4-amino-3-(4-pyridine)-5-mercapto-1,2,4-triazole with various aldehydes and/or dialdehydes. The structure of the prepared compounds was confirmed by means of 1H NMR, 13C NMR, UV-vis, IR and elemental analyses. The all prepared compounds were assayed for antibacterial (Escherichia coli and Staphylococcus aureus) and antifungal (Candida albicans) activities by disc diffusion method. The results indicate that all tested compounds did not show any antibacterial activity against E. coli, as gram negative bacteria, and antifungal activity against C. albicans. But the compounds 2, 3, 4, 6 and 8 containing 4-Cl, 4-Me, 4-MeO, 2,4-di-Cl and 2-OH substituted phenyl moiety, respectively, showed good inhibition against S. aureus as compare to standard drugs. The structure of all biologically active compounds has also been theoretically studied by ab initio Hartree-Fock (HF) methods.

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