Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C4H4N2O3 |
| Molecular Weight | 128.0862 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
O=C1CC(=O)NC(=O)N1
InChI
InChIKey=HNYOPLTXPVRDBG-UHFFFAOYSA-N
InChI=1S/C4H4N2O3/c7-2-1-3(8)6-4(9)5-2/h1H2,(H2,5,6,7,8,9)
| Molecular Formula | C4H4N2O3 |
| Molecular Weight | 128.0862 |
| 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 |
|---|---|---|
| Residual effects of temazepam and other hypnotic compounds on cognitive function. | 1980 Oct |
|
| The molecular basis of IgE antibody binding to thiopentone. Binding of IgE from thiopentone-allergic and non-allergic subjects. | 1990 Sep |
|
| Structure-activity relationship of ligands of uracil phosphoribosyltransferase from Toxoplasma gondii. | 1994 Aug 17 |
|
| Virtual combinatorial syntheses and computational screening of new potential anti-herpes compounds. | 1999 Aug 26 |
|
| Determination of barbituric acid, utilizing a rapid and simple colorimetric assay. | 2002 Jul 31 |
|
| Effect of Cd, Zn and Hg complexes of barbituric acid and thiouracil on rat brain monoamine oxidase-B (in vitro). | 2014 Feb 5 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 17:46:40 GMT 2025
by
admin
on
Mon Mar 31 17:46:40 GMT 2025
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| Record UNII |
WQ92Y2793G
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| Record Status |
Validated (UNII)
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| Record Version |
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Code | English |
| Classification Tree | Code System | Code | ||
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CFR |
21 CFR 862.3150
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7889
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31252
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DTXSID8020129
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BARBITURIC ACID
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200-658-0
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WQ92Y2793G
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m2228
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PRIMARY | Merck Index | ||
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6211
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C032232
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1279019
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67-52-7
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16294
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| Related Record | Type | Details | ||
|---|---|---|---|---|
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PARENT -> IMPURITY |
USP Peak Value = 0.15%
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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| Related Record | Type | Details | ||
|---|---|---|---|---|
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ACTIVE MOIETY |
