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Cyano-acetic acid-(3-nitro-benzylidenehydrazide) is a complex organic compound with the chemical formula C10H8N4O3. It is a derivative of cyanoacetic acid, featuring a nitrobenzylidene group attached to the hydrazide moiety. This yellow crystalline solid is known for its potential applications in the synthesis of various pharmaceuticals and chemical intermediates. The compound's structure is characterized by a cyano group (-CN), a carboxylic acid group (-COOH), and a 3-nitrobenzylidene moiety, which contributes to its reactivity and functional group diversity. Its synthesis typically involves the condensation of cyanoacetic acid with 3-nitrobenzaldehyde in the presence of a suitable catalyst, followed by the addition of a hydrazide to form the final product. Due to its unique structure, cyano-acetic acid-(3-nitro-benzylidenehydrazide) is a subject of interest in organic chemistry and medicinal chemistry research.

4980-32-9

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4980-32-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4980-32-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,8 and 0 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4980-32:
(6*4)+(5*9)+(4*8)+(3*0)+(2*3)+(1*2)=109
109 % 10 = 9
So 4980-32-9 is a valid CAS Registry Number.

4980-32-9Relevant academic research and scientific papers

7-Amino-2-aryl/hetero-aryl-5-oxo-5,8-dihydro[1,2,4]triazolo[1,5-a]pyridine-6-carbonitriles: Synthesis and adenosine receptor binding studies

Shaik, Khasim,Deb, Pran Kishore,Mailavaram, Raghu Prasad,Chandrasekaran, Balakumar,Kachler, Sonja,Klotz, Karl-Norbert,Jaber, Abdul Muttaleb Yousef

, p. 1568 - 1573 (2019/05/27)

A series of novel 7-amino-5-oxo-2-substituted-aryl/hetero-aryl-5,8-dihydro[1,2,4]triazolo[1,5-a]pyridine-6-carbonitriles (4a–4t) was synthesized, characterized and evaluated for their binding affinity and selectivity towards hA1, hA2A/sub

Microwave assisted synthesis and evaluation of N-cinnamoyl aryl hydrazones for cytotoxic and antioxidant activities

Devi, T. Sarala,Rajitha

, p. 1703 - 1709 (2016/08/06)

A series of N-cinnamoyl aryl hydrazones 2a-2i were synthesized in good yields by microwave irradiation technique. The title compounds were formed by nucleophilic condensation of various N1- substituted benzylidene-2-cyano aceto hydrazides with

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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