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1240912-46-2

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1240912-46-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1240912-46-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,0,9,1 and 2 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1240912-46:
(9*1)+(8*2)+(7*4)+(6*0)+(5*9)+(4*1)+(3*2)+(2*4)+(1*6)=122
122 % 10 = 2
So 1240912-46-2 is a valid CAS Registry Number.

1240912-46-2Upstream product

1240912-46-2Downstream Products

1240912-46-2Relevant articles and documents

Metal complexes of fenoterol drug: Preparation, spectroscopic, thermal, and biological activity characterization

Soliman,Mohamed, Gehad G.,Mohamed, Eman A.

, p. 639 - 647 (2010)

Metal complexes of fenoterol (FEN) drug are prepared and characterized based on elemental analyses, IR, 1H NMR, magnetic moment, molar conductance, and thermal analyses (TG and DTA) techniques. From the elemental analyses data, the complexes are formed in 1:2 [Metal]:[FEN] ratio and they are proposed to have the general formula [Cu(FEN)2].2H2O; [M(FEN)2(H2O)2]. yH2O (where M = Mn(II) (y = 2), Co(II) (y = 4), Ni(II) (y = 4), and Zn(II) (y = 0) and [Cr(FEN)2(H2O)2]Cl.H2O. The molar conductance data reveal that all the metal chelates are non-electrolytes except Cr(III) complex, having 1:1 electrolyte. IR spectra show that FEN is coordinated to the metal ions in a uninegative bidentate manner with ON donor sites of the aliphatic -OH and secondary amine -NH. From the magnetic moment measurements, it is found that the geometrical structures of these complexes are octahedral (Cr(III), Mn(II), Co(II), Ni(II), and Zn(II)) and square planar (Cu(II)). The thermal behavior of these chelates is studied using thermogravimetric and differential thermal analyses (TG and DTA) techniques. The results obtained show that the hydrated complexes lose water molecules of hydration followed immediately by decomposition of the coordinated water and ligand molecules in the successive unseparate steps. The FEN drug, in comparison to its metal complexes is also screened for their antibacterial activity against bacterial species (Bacillus subtilis, Staphylococcus aureus, Escherichia coli, and Salmonella typhi), Yeasts (Candida albicans and Saccharomyces cervisiae), and Fungi (Aspergillus niger and Aspergillus flavus). The activity data show that the metal complexes have antibacterial activity like that of the parent FEN drug against one or more species. Akademiai Kiado, Budapest, Hungary 2009.

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