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Hydrazinecarboxamide, 2-[(2,4-difluorophenyl)methylene]-, also known as 2-(2,4-difluorobenzylidene)hydrazinecarboxamide, is a chemical compound with the molecular formula C8H6F2N2O. It is a derivative of hydrazinecarboxamide, featuring a 2,4-difluorophenyl group attached to the methylene bridge. Hydrazinecarboxamide, 2-[(2,4-difluorophenyl)methylene]- is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of certain herbicides and antifungal agents. Its unique structure, with two fluorine atoms on the phenyl ring, contributes to its reactivity and selectivity in chemical reactions, making it a valuable building block in the development of new compounds with specific biological activities.

348-23-2

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348-23-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 348-23-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,4 and 8 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 348-23:
(5*3)+(4*4)+(3*8)+(2*2)+(1*3)=62
62 % 10 = 2
So 348-23-2 is a valid CAS Registry Number.

348-23-2Relevant academic research and scientific papers

Electrochemical synthesis of 2-amino-5-substituted-1,3,4-oxadiazole derivatives and evaluation of antibacterial activity

Kumar, Sanjeev,Pandey

, p. 252 - 258 (2013/05/09)

Some new 2-amino-5-substituted-1,3,4-oxadiazoles have been synthesized at platinum electrode through the electrochemical oxidation of semicarbazone at room temperature and studied for their antibacterial activity. This is an environmentally benign method in the field of electroorganic synthesis under controlled potential electrolysis in an undivided cell. The electrolysis have been carried out in the acetonitrile solvent and lithium perchlorate is used as a supporting electrolyte. Two platinum plates are used as working as well as counter electrode and saturated calomel electrode as the reference electrode. These compounds have been characterized by microanalyses, IR, Mass, 1H NMR and 13C NMR spectral data. All the compounds have been evaluated for their antibacterial activity against Klebsilla penumoniae, Escherichia coli, Streptococcus aureus and Shigella dysenteriea at 25 and 50 ppm concentrations.

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