Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C4H6N2O |
| Molecular Weight | 98.1032 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=CC(N)=NO1
InChI
InChIKey=FKPXGNGUVSHWQQ-UHFFFAOYSA-N
InChI=1S/C4H6N2O/c1-3-2-4(5)6-7-3/h2H,1H3,(H2,5,6)
| Molecular Formula | C4H6N2O |
| Molecular Weight | 98.1032 |
| 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 |
|---|---|---|
| Synthesis, antimicrobial, and mosquito larvicidal activity of 1-aryl-4-methyl-3,6-bis-(5-methylisoxazol-3-yl)-2-thioxo-2,3,6,10b-tetrahydro-1H-pyrimido[5,4-c]quinolin-5-ones. | 2010-10-15 |
|
| Electrochemical abatement of the antibiotic sulfamethoxazole from water. | 2010-10 |
|
| Oxidation of sulfamethoxazole by UVA radiation and modified Fenton reagent: toxicity and biodegradability of by-products. | 2009 |
|
| Synthesis, potentiometric and antimicrobial studies on metal complexes of isoxazole Schiff bases. | 2008-06 |
|
| (E)-2-Meth-oxy-6-[(5-methyl-isoxazol-3-yl)imino-meth-yl]phenol. | 2008-01-23 |
|
| Transformation of the antibacterial agent sulfamethoxazole in reactions with chlorine: kinetics, mechanisms, and pathways. | 2004-11-01 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:06:31 GMT 2025
by
admin
on
Mon Mar 31 21:06:31 GMT 2025
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| Record UNII |
G54MJS11L9
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| Record Status |
Validated (UNII)
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| Related Record | Type | Details | ||
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PARENT -> IMPURITY |
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