| Identification | Back Directory | [Name]
3-HYDROXY-2-QUINOXALINECARBOXYLIC ACID | [CAS]
1204-75-7 | [Synonyms]
NSC 34263
TIMTEC-BB SBB003659
3-HYDROXY-2-QUINOXALINECARBOXYLIC ACID
3-hydroxyquinoxaline-2-carboxylic acid
3-HYDROXY-2-QUINOXALINECARBOXYLIC ACID 98%
3-Hydroxy-2-quinoxalinecarboxylic acid,98%
3,4-Dihydro-3-oxoquinoxaline-2-carboxylic acid
3-Hydroxy-2-quinoxalinecarboxylic acid, 98% 5GR
3-hydroxyquinoxaline-2-carboxylic acid(SALTDATA: FREE) | [EINECS(EC#)]
214-877-4 | [Molecular Formula]
C9H6N2O3 | [MDL Number]
MFCD00006726 | [MOL File]
1204-75-7.mol | [Molecular Weight]
190.16 |
| Chemical Properties | Back Directory | [Appearance]
green-yellow powder and chunks | [Melting point ]
267-268 °C(lit.)
| [Boiling point ]
325.64°C (rough estimate) | [density ]
1.3907 (rough estimate) | [refractive index ]
1.5570 (estimate) | [form ]
Powder and Chunks | [pka]
0.94±0.20(Predicted) | [color ]
Green-yellow |
| Hazard Information | Back Directory | [Chemical Properties]
green-yellow powder and chunks | [Uses]
3-Hydroxy-2-quinoxalinecarboxylic acid was used to study the sorption of ionizable organic compounds to an estuarine sediment. It was used in the preparation of Zinc(II)-quinoxaline complexes which was characterized by X-ray crystallography and fluorescence spectroscopy. | [Biochem/physiol Actions]
3-Hydroxy-2-quinoxalinecarboxylic acid is an antagonist of excitatory amino acids and possesses anticonvulsant properties. It inhibits the 22Na+ efflux produced in 22Na+-preloaded brain slices by N-methyl-D-aspartate and kainate. |
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NovoChemy Ltd.
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www.novochemy.com |
| Company Name: |
Sigma-Aldrich
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https://www.sigmaaldrich.cn |
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