| Identification | More | [Name]
2,3-DIHYDROXYQUINOXALINE | [CAS]
15804-19-0 | [Synonyms]
2,3-DIHYDROXYPHENPIAZINE
2,3-DIHYDROXYQUINOXALINE
2,3-QUINOXALINEDIOL
QUINOXALINE-2,3-DIOL
TIMTEC-BB SBB000138
1,4-Dihydro-2,3-quinoxalinedione
1,4-dihydro-3-quinoxalinedione
2,3(1h,4h)-quinoxalinedione
2,3-dihydroxy-quinoxalin
2,3-Quinoxalinedione, 1,4-dihydro-
2,3-Quinoxalinedione,1,4-dihydro-
Quinoxaline, 2,3-dihydroxy-
USAF ek-6232
usafek-6232
2,3-Dihydroxyquinoxaline, 99+%
quinoxaline-2,3(1H,4H)-dione
2,3-dihydroquinoxaline
2,3(1H,4H)-Quinoxalinedione, 2,3-Quinoxalinediol | [EINECS(EC#)]
239-901-0 | [Molecular Formula]
C8H6N2O2 | [MDL Number]
MFCD00006723 | [Molecular Weight]
162.15 | [MOL File]
15804-19-0.mol |
| Chemical Properties | Back Directory | [Appearance]
off-white powder | [Melting point ]
>300 °C (lit.) | [Boiling point ]
288.82°C (rough estimate) | [density ]
1.3264 (rough estimate) | [refractive index ]
1.5770 (estimate) | [storage temp. ]
Inert atmosphere,Room Temperature | [form ]
powder to crystaline | [pka]
10.66±0.20(Predicted) | [color ]
White to Orange to Green | [BRN ]
136884 | [InChI]
InChI=1S/C8H6N2O2/c11-7-8(12)10-6-4-2-1-3-5(6)9-7/h1-4H,(H,9,11)(H,10,12) | [InChIKey]
ABJFBJGGLJVMAQ-UHFFFAOYSA-N | [SMILES]
N1C2=C(C=CC=C2)NC(=O)C1=O | [CAS DataBase Reference]
15804-19-0(CAS DataBase Reference) | [EPA Substance Registry System]
2,3-Quinoxalinedione, 1,4-dihydro- (15804-19-0) |
| Safety Data | Back Directory | [Hazard Codes ]
Xn | [Risk Statements ]
22-37/38-41 | [Safety Statements ]
S22:Do not breathe dust .
S24/25:Avoid contact with skin and eyes . | [WGK Germany ]
3
| [RTECS ]
VD2100000
| [TSCA ]
Yes | [HS Code ]
29339900 | [Storage Class]
11 - Combustible Solids | [Hazard Classifications]
Acute Tox. 4 Oral
Eye Dam. 1
Skin Irrit. 2
STOT SE 3 |
| Hazard Information | Back Directory | [Chemical Properties]
off-white powder | [Uses]
2,3-Dihydroxyquinoxaline is a fluorescent reagent and it can be used for the determination of trace Pb(II) in vinegar. | [Application]
2,3-Dihydroxyquinoxaline can be used:
(1) Basic chemical studies to determine the low-temperature x-ray molecular structure, reciprocal isomerism and spectroscopic properties of 2,3-Dihydroxyquinoxaline[1].
(2) Quinoline-5-carboxamide derivatives (Vq-Vu) and (VIa-Vu) were prepared by using methyl 2,3-diaminobenzoate as raw material[2].
| [General Description]
2,3-Dihydroxyquinoxaline(dhq) undergoes electrophilic substitution reaction with sulphuric acid solution and potassium nitrate to form 2,3-dihydroxy-6-nitroquinoxaline. It reacts with Ru3(CO)12 in DMSO to give the Ru(CO)2(dhq)(DMSO) complex. | [References]
[1] SAIED M. SOLIMAN; Morsy A M A Y; J?rg Albering. Low temperature X-ray molecular structure, tautomerism and spectral properties of 2,3-dihydroxyquinoxaline[J]. Journal of Molecular Structure, 2013. DOI:10.1016/j.molstruc.2013.09.005.
[2] KEESARI SRINIVAS. Synthesis, Characterization, and Antibacterial Activity of Novel 2,3-Dihydroxyquinoxaline-5-сarboxamide Derivatives[J]. Russian Journal of Bioorganic Chemistry, 2023. DOI:10.1134/S106816202305014X.
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