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bis(nicotinato)(triphenyl)antimony(V) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

741687-05-8

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741687-05-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 741687-05-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,1,6,8 and 7 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 741687-05:
(8*7)+(7*4)+(6*1)+(5*6)+(4*8)+(3*7)+(2*0)+(1*5)=178
178 % 10 = 8
So 741687-05-8 is a valid CAS Registry Number.

741687-05-8Downstream Products

741687-05-8Relevant academic research and scientific papers

Synthesis, characterization and antileishmanial studies of some bioactive heteroleptic pentavalent antimonials

Mushtaq, Rabia,Rauf, Muhammad Khawar,Bolte, Michael,Nadhman, Akhtar,Badshah, Amin,Tahir, Muhammad Nawaz,Yasinzai, Masoom,Khan, Khalid Mohammed

, (2017/04/21)

In pursuit of safe drug candidates for the treatment of parasitic diseases like leishmaniasis, a series of heteroleptic pentavalent antimonials of the type [R3Sb(O2CR′)2] (1–9) have been synthesized and characterized using elemental analysis (CHN), Fourier transform infrared spectroscopy and multinuclear (1H and 13C) NMR spectroscopy. The carboxylates studied are predominantly substituted benzoates with some complexes having acetato or nicotinato ligands. The crystal structures of [Sb(C6H5)3(o-NH2C6H4COO)2] (1) and [Sb(C6H5)3(3,5-Cl2C6H3COO)2] (4) were determined as essentially monomeric with an Sb(V) centre and shown to adopt geometries intermediate between trigonal bipyramidal and square pyramidal. The antileishmanial activity was assessed against Leishmania tropica KWH23, and also human macrophages were used to measure the cytotoxicity of these complexes. The IC50 of the antimonials 1–9 indicates their efficaciousness as compared with the standard antimonial drug used. The significant activity of complex 1 assumes that greater multitude of interactions is the cause of enhanced antileishmanial activity. Cytotoxicity results showed that these antimonials are highly active even at low concentrations and are biocompatible with human macrophages, making them promising drug candidates for further investigations in this field.

Synthesis and structure of tetraphenylantimony nicotinate

Sharutin,Pakusina,Platonova,Sharutina,Gerasimenko,Popov,Pushilin

, p. 207 - 210 (2007/10/03)

Tetraphenylantimony nicotinate was prepared in 91% yield by reaction of pentaphenylantimony with triphenylantimony bis(nicotinate) in toluene. Triphenylantimony bis(nicotinate), in turn, was prepared in 87% yield by oxidative addition of pyridine-3-carboxylic acid to triphenylstibine in ether in the presence of hydrogen peroxide. The structure of tetraphenylantimony nicotinate was determined by single-crystal X-ray diffraction. The Sb atom has a distorted trigonal bipyramidal coordination surrounding with the carboxy group in the axial position. The Sb-C distances are 2.118(1), 2.121(1), 2.130(1), and 2.170(1) A, and the Sb-O distance is 2.268(1) A. There is an intramolecular contact between the Sb atom and the carbonyl O atom [3.363(1) A].

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