quinoline n-oxide hydrate structure
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Common Name | quinoline n-oxide hydrate | ||
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| CAS Number | 64201-64-5 | Molecular Weight | 163.17300 | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | C9H9NO2 | Melting Point | 52-55 °C(lit.) | |
| MSDS | USA | Flash Point | >230 °F | |
| Name | 1-oxidoquinolin-1-ium,hydrate |
|---|---|
| Synonym | More Synonyms |
| Melting Point | 52-55 °C(lit.) |
|---|---|
| Molecular Formula | C9H9NO2 |
| Molecular Weight | 163.17300 |
| Flash Point | >230 °F |
| Exact Mass | 163.06300 |
| PSA | 34.69000 |
| LogP | 2.20400 |
| Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
|---|---|
| Hazard Codes | Xi |
| Risk Phrases | R36/38:Irritating to eyes and skin . |
| Safety Phrases | S22-S24/25 |
| RIDADR | NONH for all modes of transport |
| WGK Germany | 3 |
| RTECS | VC2340000 |
| HS Code | 2933499090 |
| HS Code | 2933499090 |
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| Summary | 2933499090. other compounds containing in the structure a quinoline or isoquinoline ring-system (whether or not hydrogenated), not further fused. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
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Direct, catalytic, and regioselective synthesis of 2-alkyl-, aryl-, and alkenyl-substituted N-heterocycles from N-oxides.
Org. Lett. 16(3) , 864-7, (2014) A one-step transformation of heterocyclic N-oxides to 2-alkyl-, aryl-, and alkenyl-substituted N-heterocycles is described. The success of this broad-scope methodology hinges on the combination of cop... |
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Lanthanide chloride complexes with quinoline-n-oxide. Kingston JV, et al.
J. Inorg. Nucl. Chem. 31(10) , 3181-3185, (1969)
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The application of trifluoroacetic anhydride-sodium iodide (TFAA-I) system for quantitative determination of nitrones. Clesielski W, et al.
Can. J. Chem. 68(5) , 679-684, (1990)
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| Quinoline N-oxide hydrate |
| quinolinol,oxamethane |
| EINECS 216-560-6 |
| MFCD00149472 |
| 1-oxidoquinolin-1-ium hydrate |
| quinoline 1-oxide monohydrate |