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5-(4-chlorophenyl)-3-(5-nitrofuran-2-yl)isoxazole is a complex organic chemical compound with the molecular formula C12H6ClN3O4. It is characterized by the presence of a 4-chlorophenyl group attached to the 5-position of an isoxazole ring, and a 5-nitrofuran-2-yl group at the 3-position. 5-(4-chlorophenyl)-3-(5-nitrofuran-2-yl)isoxazole is known for its potential applications in the pharmaceutical industry, particularly as an intermediate in the synthesis of various drugs. Its structure features a chlorine atom, which can participate in various chemical reactions, and a nitro group, which is known for its reactivity and can be reduced to form different functional groups. The compound's properties, such as its solubility, stability, and reactivity, are influenced by the presence of these functional groups, making it a versatile building block in organic synthesis.

7204-89-9

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7204-89-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7204-89-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,0 and 4 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7204-89:
(6*7)+(5*2)+(4*0)+(3*4)+(2*8)+(1*9)=89
89 % 10 = 9
So 7204-89-9 is a valid CAS Registry Number.

7204-89-9Downstream Products

7204-89-9Relevant academic research and scientific papers

Design, synthesis, antileishmanial, and antifungal biological evaluation of novel 3,5-disubstituted isoxazole compounds based on 5-nitrofuran scaffolds

Trefzger, Ozildéia S.,Barbosa, Natália V.,Scapolatempo, Renata L.,das Neves, Amarith R.,Ortale, Maria L. F. S.,Carvalho, Diego B.,Honorato, Ant?nio M.,Fragoso, Mariana R.,Shuiguemoto, Cristiane Y. K.,Perdomo, Renata T.,Matos, Maria F. C.,Chang, Marilene R.,Arruda, Carla C. P.,Baroni, Adriano C. M.

, (2020)

Nineteen 3,5-disubstituted-isoxazole analogs were synthesized based on nitrofuran scaffolds, by a [3 + 2] cycloaddition reaction between terminal acetylenes and 5-nitrofuran chloro-oxime. The compounds were obtained in moderate to very good yields (45–91%). The antileishmanial activity was assayed against the promastigote and amastigote forms of Leishmania (Leishmania) amazonensis. Alkylchlorinated compounds 14p–r were active on both the promastigote and amastigote forms, with emphasis on compound 14p, which showed strong activity against the amastigote form (IC50 = 0.6 μM and selectivity index [SI] = 5.2). In the alkyl series, compound 14o stands out with an IC50 = 8.5 μM and SI = 8.0 on the amastigote form. In the aromatic series, the most active compounds were those containing electron-donor groups, such as trimethoxy isoxazole 14g (IC50 = 1.2 μM and SI = 20.2); compound 14h, with IC50 = 7.0 μM and SI = 6.1; and compound 14j containing the 4-SCH3 group, with IC50 = 5.7 μM and SI = 10.2. In addition, the antifungal activity of 19 nitrofuran isoxazoles was evaluated against five strains of Candida (C. albicans, C. parapsilosis, C. krusei, C. tropicalis, and C. glabrata). Eleven isoxazole derivatives were active against C. parapsilosis, and compound 14o was found to be the most active (minimal inhibitory concentration [MIC] = 3.4 μM) for this strain. Compound 14p was active against all the strains tested, with an MIC = 17.5 μM for C. glabrata, lower than that of the fluconazole used as the reference drug.

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