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1‐(α‐ferrocenylbenzyl)imidazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

654083-47-3

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654083-47-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 654083-47-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,4,0,8 and 3 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 654083-47:
(8*6)+(7*5)+(6*4)+(5*0)+(4*8)+(3*3)+(2*4)+(1*7)=163
163 % 10 = 3
So 654083-47-3 is a valid CAS Registry Number.

654083-47-3Downstream Products

654083-47-3Relevant academic research and scientific papers

Synthesis, structure and redox potentials of biologically active ferrocenylalkyl azoles

Snegur, Lubov V.,Simenel, Alexander A.,Nekrasov, Yury S.,Morozova, Elena A.,Starikova, Zoya A.,Peregudova, Svetlana M.,Kuzmenko, Yuliya V.,Babin, Valery N.,Ostrovskaya, Larissa A.,Bluchterova, Natalia V.,Fomina, Margarita M.

, p. 2473 - 2479 (2004)

The syntheses, structures, electrochemical properties of the series of ferrocenylalkyl azoles, FcAlkAz, as well as the antitumor activity of ferrocenylmethyl benzimidazole (8) have been studied. Above mentioned compounds were investigated by the method of cyclic voltametry. All of them exhibited a reversible one-electron oxidation-reduction wave owing to the ferrocene-ferrocenium redox couple with a positive shift (0.50-0.65 V) compared with that of ferrocene (0.42 V). The X-ray determination of molecular structures of 1-(ferrocenylmethyl)imidazole (4), 1-(ferrocenylbenzyl)imidazole (7) and 1-(ferrocenylmethyl)bezimidazole (8) was carried out. Compound 4 with imidazolyl substituent was found to be present in N-protonated form. Antitumor activity of 1-(ferrocenylmethyl)benzimidazole (8) against some solid tumor models such as adenocarcinoma 755 (Ca755), melanoma B16 (B16) and Lewis lung carcinoma was studied. The antitumor activity of compound 8 was compared with cisplatin effectiveness against some experimental tumor systems.

Solvent-free reactions of N,N′-thiocarbonyldiimidazole with ferrocenylcarbinols

Onyancha, Douglas,Nyamori, Vincent,McCleland, Cedric W.,Imrie, Christopher,Gerber, Thomas I.A.

, p. 207 - 212 (2009/04/13)

The efficient and simple routes for the synthesis of various ferrocenyl derivatives from ferrocenylcarbinols and N,N′-thiocarbonyldiimidazole (TCDI) are described. It involves grinding the two substrates in a Pyrex tube with a glass rod at room temperatur

Synthesis and enantiomeric resolution of ferrocenyl(alkyl)azoles

Simenel, Alexander A.,Kuzmenko, Yulia V.,Morozova, Elena A.,Ilyin, Mikhail M.,Gun'ko, Irina F.,Snegur, Lubov' V.

, p. 138 - 143 (2007/10/03)

Ferrocenyl(alkyl)azoles were synthesized in high yields by interaction of α-ferrocenylcarbinoles with azoles in aqueous-organic in the presence of HBF4 or by interaction of α-ferrocenylcarbinoles with N,N′-carbonyldiimidazole, N,N′-thionyldiimi

Simple route to ferrcenyl(alkyl)imidazoles

Simenel, Alexander A.,Morozova, Elena A.,Kuzmenko, Yulia V.,Snegur, Lubov' V.

, p. 13 - 14 (2007/10/03)

A suitable method for the synthesis of ferrocenyl(alkyl)imidazoles is proposed. The treatment of α-ferrocenylcarbinols with N,N′-carbonyldiimidazole affords the title compounds, are in more than 80% yields.

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