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3-(2-(methylthio)phenylazo)-2,4-pentanedione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1304495-19-9

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1304495-19-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1304495-19-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,0,4,4,9 and 5 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1304495-19:
(9*1)+(8*3)+(7*0)+(6*4)+(5*4)+(4*9)+(3*5)+(2*1)+(1*9)=139
139 % 10 = 9
So 1304495-19-9 is a valid CAS Registry Number.

1304495-19-9Downstream Products

1304495-19-9Relevant academic research and scientific papers

Structures, redox behavior, antibacterial activity and correlation with electronic structure of the complexes of nickel triad with 3-(2-(alkylthio) phenylazo)-2,4-pentanedione

Paira, Mrinal Kanti,Mondal, Tapan Kumar,Ojha, Durbadal,Slawin, Alexandra M.Z.,Tiekink, Edward R.T.,Samanta, Amalesh,Sinha, Chittaranjan

, p. 175 - 186 (2011)

3-(2-(Alkylthio)phenylazo)-2,4-pentanedione (HL), an O, N, S donor ligand, is used for the synthesis of Ni(II), Pd(II) and Pt(II) complexes. The spectroscopic (IR, UV-Vis, and NMR) data determine the structure. The single crystal X-ray diffraction measurement of [Ni(L)2] and [Pt(L)Cl] has confirmed the structures. Coulometric oxidation of [Ni(L)2] and EPR spectra thereof show formation of Ni(III) state. DFT computation has calculated the electronic configuration and has explained the spectral and redox properties of the complexes. The compounds are screened for their in vitro anti-bacterial activity using Gram-positive and Gram-negative bacteria (Bacillus subtilis UC564, Escherichia coli TG1, Staphylococcus aureus Bang25, Pseudomonas aeruginosa C/1/7, Salmonella typhi NCTC62, Salmonella paratyphi NCTC A2, Shigella dysenteriae 8NCTC599/52, Streptococcus faecalis S2, Vibrio cholerae DN7 and Mricococcus luteus AGD1). The minimum inhibitory concentration is determined for the compounds. The effect of the structure of the investigated compounds on the antibacterial activity is discussed.

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