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N'‐[(4‐chlorophenyl)methylidene]‐5‐nitrofuran‐2‐carbohydrazide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

29448-95-1

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29448-95-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29448-95-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,4,4 and 8 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 29448-95:
(7*2)+(6*9)+(5*4)+(4*4)+(3*8)+(2*9)+(1*5)=151
151 % 10 = 1
So 29448-95-1 is a valid CAS Registry Number.

29448-95-1Downstream Products

29448-95-1Relevant academic research and scientific papers

Synthesis of promising antimicrobial agents: hydrazide-hydrazones of 5-nitrofuran-2-carboxylic acid

Popio?ek, ?ukasz,Rysz, Bernadetta,Biernasiuk, Anna,Wujec, Monika

, p. 260 - 269 (2019/11/14)

In this research, we synthesized and evaluated for in vitro antimicrobial activity a new series of hydrazide-hydrazones obtained from 5-nitrofuran-2-carboxylic acid. New compounds were identified and characterized by spectral methods (1H NMR and 13C NMR). All tested hydrazide-hydrazones proved to be promising antimicrobial agents. Antimicrobial activity and antifungal activity of new derivatives of 5-nitrofuran-2-carboxylic acid were revealed in many cases to be higher than the activity of reference substances (nitrofurantoin, cefuroxime and ampicillin).

5-Nitro-2-furoic acid hydrazones: Design, synthesis and in vitro antimycobacterial evaluation against log and starved phase cultures

Sriram, Dharmarajan,Yogeeswari, Perumal,Vyas, Devambatla Ravi Kumar,Senthilkumar, Palaniappan,Bhat, Pritesh,Srividya, Madala

scheme or table, p. 4313 - 4316 (2010/09/18)

Various 5-nitro-2-furoic acid hydrazones were synthesized and evaluated for in vitro activities against log and starved phase culture of two mycobacterial species and Mycobacterium tuberculosis (MTB) isocitrate lyase (ICL) enzyme inhibition studies. Among twenty one compounds, 5-nitro-N′-[(5-nitro-2- furyl)methylidene]-2-furohydrazide (4o) was found to be the most active compound in vitro with MICs of 2.65 and 10.64 μM against log- and starved-phase culture of MTB. Compound 4o also showed good enzyme inhibition of MTB ICL at 10 μM. The docking studies also confirmed the binding potential of the compounds at the ICL active site.

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