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79602-39-4

(E)-(2-((2-hydroxybenzylidene)amino)phenyl)(phenyl)methanone (E)-(2-((2-hydroxybenzylidene)amino)phenyl)(phenyl)methanone is a tridentate Schiff base ligand derived from the condensation of 2-aminobenzophenone with 2-hydroxybenzaldehyde. It forms stable square planar metal(II) chelates, which exhibit non-electrolytic behavior and demonstrate significant DNA-binding properties through intercalation, as well as notable antimicrobial and catalytic activities, particularly in the oxidation of toluene to benzaldehyde. The ligand and its metal complexes were structurally characterized using spectroscopic and analytical techniques, confirming their stoichiometry and geometric arrangements.

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  • 79602-39-4 Structure

  • Basic information

    1. Product Name: (E)-(2-((2-hydroxybenzylidene)amino)phenyl)(phenyl)methanone
    2. Synonyms: (E)-(2-((2-hydroxybenzylidene)amino)phenyl)(phenyl)methanone
    3. CAS NO:79602-39-4
    4. Molecular Formula:
    5. Molecular Weight: 301.345
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 79602-39-4.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: (E)-(2-((2-hydroxybenzylidene)amino)phenyl)(phenyl)methanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-(2-((2-hydroxybenzylidene)amino)phenyl)(phenyl)methanone(79602-39-4)
    11. EPA Substance Registry System: (E)-(2-((2-hydroxybenzylidene)amino)phenyl)(phenyl)methanone(79602-39-4)

  • 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: 79602-39-4(Hazardous Substances Data)

79602-39-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79602-39-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,6,0 and 2 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 79602-39:
(7*7)+(6*9)+(5*6)+(4*0)+(3*2)+(2*3)+(1*9)=154
154 % 10 = 4
So 79602-39-4 is a valid CAS Registry Number.

79602-39-4Downstream Products

79602-39-4Relevant articles and documents

Synthesis, structural characterization, in-vitro antibiogram assay and efficient catalytic activities of transition metal(II) chelates incorporating (E)-(2-((2-hydroxybenzylidene)amino)phenyl)(phenyl)methanone ligand

Muniyandi, Vellaichamy,Pravin, Narayanaperumal,Mitu, Liviu,Raman, Natarajan

, p. 56 - 63 (2015)

A new tridentate ligand, (E)-(2-((2-hydroxybenzylidene)amino)phenyl)(phenyl)methanone and its four metal(II) chelates have been designed and synthesized. They were structurally characterized by elemental analysis, FT IR, UV-vis, 1H NMR, 13C NMR, mass spectra, EPR, magnetic moment and conductivity measurements. Elemental analysis and molar conductance values reveal that all the chelates are 1:1 stoichiometry of the type [MLCl] having non-electrolytic nature. The metal chelates adopt square planar geometrical arrangements around the metal ions. The DNA-binding properties of these chelates have been investigated by electronic absorption, cyclic voltammetry, differential pulse voltammogram and viscosity measurements. The data indicate that these complexes bind to DNA via an intercalation mode. The oxidative cleavage of the metal complexes with pBR322 DNA has also been investigated by gel electrophoresis. Moreover, the antimicrobial bustle shows that all metal chelates have superior activity than the free ligand. The oxidation of toluene to benzaldehyde is effectively catalyzed by the synthesized chelates.

Impact of metallonucleases on DNA interactions: Structural validation and in-vitro antibiogram assay

Muniyandi, Vellaichamy,Pravin, Narayanaperumal,Raman, Natarajan

, p. 60 - 64 (2014)

Four novel complexes were synthesized using 2-aminobenzophenone Schiff base precursor and characterized by various analytical techniques. FT-IR results demonstrate that the Schiff base ligand, obtained by the condensation of 2-aminobenzophenone with 2-hyd

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