736-53-8 Usage
Description
5-Nitro-2-furaldehyde (5-nitrofurfurylene)hydrazone is an organic compound with the molecular formula C5H4N4O3. It is a derivative of 5-nitrofurfural, which is known for its various biological activities. 5-nitro-2-furaldehyde (5-nitrofurfurylene)hydrazone is characterized by its nitro group and hydrazone functional group, which contribute to its potential applications in different fields.
Uses
Used in Pharmaceutical Industry:
5-Nitro-2-furaldehyde (5-nitrofurfurylene)hydrazone is used as an active pharmaceutical ingredient for the development of drugs with antibacterial, antifungal, and antiprotozoal properties. Its broad-spectrum action makes it effective against various pathogens, including Chlamydia trachomatis, Mycoplasma spp., and Candida spp.
Used in Antimicrobial Applications:
In the field of antimicrobials, 5-Nitro-2-furaldehyde (5-nitrofurfurylene)hydrazone is utilized as a potent agent against a wide range of bacteria, fungi, and protozoa. Its ability to target multiple pathogens makes it a valuable compound in the development of new antimicrobial drugs to combat drug-resistant infections.
Used in Research and Development:
5-Nitro-2-furaldehyde (5-nitrofurfurylene)hydrazone is also used as a research compound in the study of its chemical properties, synthesis methods, and potential applications in various industries. Its unique structure and functional groups make it an interesting subject for further investigation and development of new compounds with improved properties and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 736-53-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,3 and 6 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 736-53:
(5*7)+(4*3)+(3*6)+(2*5)+(1*3)=78
78 % 10 = 8
So 736-53-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H6N4O6/c15-13(16)9-3-1-7(19-9)5-11-12-6-8-2-4-10(20-8)14(17)18/h1-6H/b11-5+,12-6+
736-53-8Relevant articles and documents
Synthesis, protolytic equilibria, and antimicrobial action of nifuroxazide analogs
Gamov,Kiselev,Murekhina,Zavalishin,Aleksandriiskii,Kosterin, D.Yu.
, (2021/07/16)
The present paper reports on the synthesis of four hydrazones derived from 5-nitro-2-furfural, 5-nitro-2-thiophenal, isoniazid, 2,4- and 3,4-dihydroxy-N′-methylenebenzohydrazide. The acid-base dissociation constants of these compounds were determined in an aqueous solution. The protolytic equilibria-related ability of hydrazones to “sense” anions in dimethyl sulfoxide-containing water of different concentrations is studied using spectrophotometry, NMR spectroscopy, and quantum chemistry methods. The antimicrobial action of the hydrazones was tested and compared with that of the known drug nifuroxazide.
