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1-[2-(2,3-dicyanophenoxy)ethyl]-2-methyl-5-nitro-1H-imidazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1456891-14-7

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1456891-14-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1456891-14-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,6,8,9 and 1 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1456891-14:
(9*1)+(8*4)+(7*5)+(6*6)+(5*8)+(4*9)+(3*1)+(2*1)+(1*4)=197
197 % 10 = 7
So 1456891-14-7 is a valid CAS Registry Number.

1456891-14-7Downstream Products

1456891-14-7Relevant academic research and scientific papers

Phthalocyanines functionalized with 2-methyl-5-nitro-1H-imidazolylethoxy and 1,4,7-trioxanonyl moieties and the effect of metronidazole substitution on photocytotoxicity

Wierzchowski, Marcin,Sobotta, Lukasz,Skupin-Mrugalska, Paulina,Kruk, Justyna,Jusiak, Weronika,Yee, Michael,Konopka, Krystyna,Düzgüne?, Nejat,Tykarska, Ewa,Gdaniec, Maria,Mielcarek, Jadwiga,Goslinski, Tomasz

, p. 62 - 72 (2013)

Four novel magnesium(II) and zinc(II) phthalocyanines bearing 1,4,7-trioxanonyl, polyether and/or (2-methyl-5-nitro-1H-imidazol-1-yl)ethoxy, heterocyclic substituents at their non-peripheral positions were synthesized and assessed in terms of physicochemical and biological properties. Magnesium phthalocyanine derivatives bearing polyether substituents (Pc-1), a mixed system of polyether and heterocyclic substituents (Pc-3), and four heterocyclic substituents (Pc-4), respectively, were synthesized following the Linstead macrocyclization reaction procedure. Zinc phthalocyanine (Pc-2) bearing polyether substituents at non-peripheral positions was synthesized following the procedure in n-pentanol with the zinc acetate, and DBU. Novel phthalocyanines were purified by flash column chromatography and characterized using NMR, MS, UV-Vis and HPLC. Moreover, two precursors in macrocyclization reaction phthalonitriles were characterized using X-ray. Photophysical properties of the novel macrocycles were evaluated, including UV-Vis spectra analysis and aggregation study. All macrocycles subjected to singlet oxygen generation and the oxidation rate constant measurements exhibited lower quantum yields of singlet oxygen generation in DMSO than in DMF. In addition, the Pc-2 molecule was found to be the most efficient singlet oxygen generator from the group of macrocycles studied. The photocytotoxicity evaluated on the human oral squamous cell carcinoma cell line, HSC-3, for Pc-3 was significantly higher than that for Pc-1, Pc-2, and Pc-4. Interestingly, Pc-3 was found to be the most active macrocycle in vitro although its ability to generate singlet oxygen was significantly lower than those of Pc-1 and Pc-2. However, attempts to encapsulate phthalocyanines Pc-1-Pc-3 in liposomal membranes were unsuccessful. The phthalocyanine-nitroimidazole conjugate, Pc-4 was encapsulated in phosphatidylglycerol:phosphatidylcholine unilamellar liposomes and subjected to photocytotoxicity study.

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