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N'-(3-NITROBENZYLIDENE)ISONICOTINOHYDRAZIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

16012-26-3

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16012-26-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16012-26-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,0,1 and 2 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 16012-26:
(7*1)+(6*6)+(5*0)+(4*1)+(3*2)+(2*2)+(1*6)=63
63 % 10 = 3
So 16012-26-3 is a valid CAS Registry Number.

16012-26-3Downstream Products

16012-26-3Relevant academic research and scientific papers

Xanthine oxidase inhibitory activity of nicotino/isonicotinohydrazides: A systematic approach from in vitro, in silico to in vivo studies

Zafar, Humaira,Hayat, Muhammad,Saied, Sumayya,Khan, Momin,Salar, Uzma,Malik, Rizwana,Choudhary, M. Iqbal,Khan, Khalid Mohammed

, p. 2351 - 2371 (2017/04/03)

Change in life style and eating habits has led to an increased prevalence of hyperuricemia worldwide. The role of hyperuricemia is no more restricted to gout, but it has a central role in progression of CVD, hypertension, metabolic syndrome, and arthritis

Isonicotinohydrazones as inhibitors of alkaline phosphatase and ecto-5′-nucleotidase

Channar, Pervaiz Ali,Shah, Syed Jawad Ali,Hassan, Sidra,Nisa, Zaib un,Lecka, Joanna,Sévigny, Jean,Bajorath, Jürgen,Saeed, Aamer,Iqbal, Jamshed

, p. 365 - 370 (2017/04/03)

A series of isonicotinohydrazide derivatives was synthesized and tested against recombinant human and rat ecto-5′-nucleotidases (h-e5′NT and r-e5′NT) and alkaline phosphatase isozymes including both bovine tissue-non-specific alkaline phosphatase (b-TNAP)

Synthesis, characterization and pharmacological evaluation of (E)-N′-(substituted-benzylidene)isonicotinohydrazide derivatives as potent anticonvulsant agents

Malhotra, Manav,Monga, Vikramdeep,Sharma, Sagun,Jain, Jainendra,Samad, Abdul,Stables, James,Deep, Aakash

, p. 2145 - 2152 (2012/11/07)

A series of (E)-N′-(substituted-benzylidene)isonicotinohydrazide derivatives were synthesized by coupling it with different substituted aldehydes, acetophenone, and benzophenones in presence of absolute ethanol along with catalytic amount of glacial aceti

Synthesis and anti-mycobacterial activity of (E)-N′-(monosubstituted-benzylidene)isonicotinohydrazide derivatives

Lourenco, Maria Cristina da Silva,Ferreira, Marcelle de Lima,de Souza, Marcus Vinicius Nora,Peralta, Monica Amado,Vasconcelos, Thatyana Rocha Alves,Henriques, Maria das Gracas M.O.

, p. 1344 - 1347 (2008/09/21)

A series of 22 (E)-N′-(monosubstituted-benzylidene)isonicotinohydrazide derivatives have been synthesized and evaluated for their in vitro antibacterial activity against Mycobacterium tuberculosis H37Rv using Alamar Blue susceptibility test and

Four nitrobenzaldehyde isonicotinoyl-hydrazones at 120 K: Four different supramolecular structures in two and three dimensions

Wardell, Solange M. S. V.,De Souza, Marcus V. N.,Wardell, James L.,Low, John N.,Glidewell, Christopher

, p. o683-o689 (2007/10/03)

The molecules of 2-nitrobenzaldehyde isonicotinoylhydra-zone, C 13H10N4O3, (I), are linked into a three-dimensional framework by a combination of one N-H...N and three C-H...O hydrogen bonds. In the isomeric com

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