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N′-(2-hydroxy-5-nitrophenyl-methylidene)-3-pyridincarbohydrazide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

41377-69-9

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41377-69-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41377-69-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,3,7 and 7 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 41377-69:
(7*4)+(6*1)+(5*3)+(4*7)+(3*7)+(2*6)+(1*9)=119
119 % 10 = 9
So 41377-69-9 is a valid CAS Registry Number.

41377-69-9Downstream Products

41377-69-9Relevant academic research and scientific papers

Acid–Base Properties and Kinetics of Hydrolysis of Aroylhydrazones Derived from Nicotinic Acid Hydrazide

Benkovi?,Kontrec,Tomi?i?,Budimir,Gali?

, p. 1227 - 1245 (2016)

A series of aroylhydrazones were synthesized from nicotinic acid hydrazide and differently substituted benzaldehydes. The protonation constants of the 12 resulting hydrazones, as well as of the starting compounds, were determined in methanol/water 1/1 mix

Characterization and antidiabetic activity of salicylhydrazone Schiff base vanadium(IV) and (V) complexes

Szklarzewicz, Janusz,Jurowska, Anna,Hodorowicz, Maciej,Kazek, Grzegorz,Mordyl, Barbara,Menaszek, El?bieta,Sapa, Jacek

, p. 201 - 217 (2020/12/28)

Twenty-four oxidovanadium(IV,V) complexes with tridentate Schiff base ligands based on 5-nitrosalicylaldehyde, 5-methoxysalicylaldehyde, or 5-sulfosalicylaldehyde and respective hydrazide were isolated, and characterized using physicochemical and spectros

Copper(II) complexes of aroylhydrazones: Preparation and structural characterization

Ken?el, Adriana,Miljani?, Sne?ana,Kontrec, Darko,Soldin, ?eljka,Gali?, Nives

, (2020/02/03)

Structures of solid copper complexes with aroylhydrazones obtained from nicotinic acid hydrazide and salicylaldehyde derivatives differing in substituents on the benzene ring were analysed by means of infrared (IR) and Raman spectroscopy. Studied aromatic

Potent antimicrobial agents against azole-resistant fungi based on pyridinohydrazide and hydrazomethylpyridine structural motifs

Backes, Gregory L.,Jursic, Branko S.,Neumann, Donna M.

, p. 3397 - 3407 (2015/08/03)

Abstract Schiff base derivatives have recently been shown to possess antimicrobial activity, and these derivatives include a limited number of salicylaldehyde hydrazones. To further explore this structure-activity relationship between salicylaldehyde hydrazones and antifungal activity, we previously synthesized and analyzed a large series of salicylaldehyde and formylpyridinetrione hydrazones for their ability to inhibit fungal growth of both azole-susceptible and azole-resistant species of Candida. While many of these analogs showed excellent growth inhibition with low mammalian cell toxicity, their activity did not extend to azole-resistant species of Candida. To further dissect the structural features necessary to inhibit azole-resistant fungal species, we synthesized a new class of modified salicylaldehyde derivatives and subsequently identified a series of modified pyridine-based hydrazones that had potent fungicidal antifungal activity against multiple Candida spp. Here we would like to present our synthetic procedures as well as the results from fungal growth inhibition assays, mammalian cell toxicity assays, time-kill assays and synergy studies of these novel pyridine-based hydrazones on both azole-susceptible and azole-resistant fungal species.

Mechanistic differences between in vitro assays for hydrazone-based small molecule inhibitors of anthrax lethal factor

Hanna, M. Leslie,Tarasow, Theodore M.,Perkins, Julie

, p. 50 - 58 (2008/09/18)

A systematically generated series of hydrazones were analyzed as potential inhibitors of anthrax lethal factor. The hydrazones were screened using one UV-based and two fluorescence-based in vitro assays. The study identified several inhibitors with IC50 values in the micromolar range, and importantly, significant differences in the types of inhibition were observed with the different assays.

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