CAS 5579-89-5
:1-Ethyl-2-[(5-nitro-2-furanyl)methylene]hydrazinecarboxamide
Description:
1-Ethyl-2-[(5-nitro-2-furanyl)methylene]hydrazinecarboxamide, with the CAS number 5579-89-5, is a chemical compound that belongs to the class of hydrazine derivatives. It features a hydrazinecarboxamide functional group, which is characterized by the presence of a hydrazine moiety (–NH–NH2) linked to a carboxamide (–C(=O)NH2) group. The compound also contains a furan ring substituted with a nitro group, which contributes to its potential reactivity and biological activity. The ethyl group enhances its lipophilicity, potentially influencing its solubility and interaction with biological membranes. This compound may exhibit various pharmacological properties, making it of interest in medicinal chemistry. Its structural features suggest potential applications in drug development, particularly in targeting specific biological pathways. However, detailed studies on its toxicity, stability, and specific applications would be necessary to fully understand its characteristics and potential uses in various fields, including pharmaceuticals and agrochemicals.
Formula:C8H10N4O4
InChI:InChI=1/C8H10N4O4/c1-2-11(8(9)13)10-5-6-3-4-7(16-6)12(14)15/h3-5H,2H2,1H3,(H2,9,13)/b10-5+
InChI key:InChIKey=JGPNCLKRECLYTO-UHFFFAOYSA-N
SMILES:C(=NN(C(N)=O)CC)C=1OC(N(=O)=O)=CC1
Synonyms:- (2E)-1-ethyl-2-[(5-nitrofuran-2-yl)methylidene]hydrazinecarboxamide
- 1-Ethyl-2-[(5-nitro-2-furanyl)methylene]hydrazinecarboxamide
- 2-Furaldehyde, 5-nitro-, 2-ethylsemicarbazone
- 5-Nitro-2-furaldehyde 2-ethylsemicarbazone
- Etafurazone
- Hydrazinecarboxamide, 1-ethyl-2-[(5-nitro-2-furanyl)methylene]-
- NSC 186580
- Nf 161
- Nifursemizone
- 5-Nitro-2-furancarbaldehyde 2-ethyl semicarbazone
- See more synonyms
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Found 3 products.
Nifursemizone
CAS:Nifursemizone (Etafurazone) is an agent with antiprotozoal.Formula:C8H10N4O4Purity:99.57%Color and Shape:SolidMolecular weight:226.19Nifursemizone
CAS:<p>Nifursemizone is an antimicrobial agent, which is a synthetic nitrofuran derivative. It is engineered from chemical precursors through targeted synthetic processes designed to maximize its antibacterial properties. The mode of action of Nifursemizone involves the inhibition of bacterial enzymes and interference with nucleic acid synthesis. This action disrupts essential bacterial functions, leading to the inhibition of bacterial growth and eventual cell death.</p>Formula:C8H10N4O4Purity:Min. 95%Molecular weight:226.19 g/mol


