Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C5H3NO4 |
| Molecular Weight | 141.0816 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[O-][N+](=O)C1=CC=C(O1)C=O
InChI
InChIKey=SXINBFXPADXIEY-UHFFFAOYSA-N
InChI=1S/C5H3NO4/c7-3-4-1-2-5(10-4)6(8)9/h1-3H
| Molecular Formula | C5H3NO4 |
| Molecular Weight | 141.0816 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Design, synthesis, and biological evaluation of 4-(5-nitrofuran-2-yl)prop-2-en-1-one derivatives as potent antitubercular agents. | 2010-11-01 |
|
| Broad specificity indirect competitive immunoassay for determination of nitrofurans in animal feeds. | 2010-09-23 |
|
| Simultaneous extraction and preconcentration of uranium and thorium in aqueous samples by new modified mesoporous silica prior to inductively coupled plasma optical emission spectrometry determination. | 2009-11-15 |
|
| Platinum-based complexes of bioactive 3-(5-nitrofuryl)acroleine thiosemicarbazones showing anti-Trypanosoma cruzi activity. | 2009-03 |
|
| Semicarbazide is non-specific as a marker metabolite to reveal nitrofurazone abuse as it can form under Hofmann conditions. | 2009-01 |
|
| The scale-free dynamics of eukaryotic cells. | 2008 |
|
| Synthesis of heteroaryl imines: theoretical and experimental approach to the determination of the configuration of C=N double bond. | 2006-09-15 |
|
| Synthesis and preliminary screening of carbohydrazides and hydrazones of pyrrole derivatives as potential tuberculostatics. | 2006 |
|
| GLR1 plays an essential role in the homeodynamics of glutathione and the regulation of H2S production during respiratory oscillation of Saccharomyces cerevisiae. | 2005-12 |
|
| Reactivity of 5-nitro-2-furaldehyde in alkaline and acidic solutions. | 2002-08-29 |
|
| Structure-activity relationships of hydrazono derivatives of biological interest. | 1989-04 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
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Mon Mar 31 19:19:54 GMT 2025
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on
Mon Mar 31 19:19:54 GMT 2025
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XXX18AU0Z3
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