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关于此项目
经验公式(希尔记法):
C9H7NO · xH2O
化学文摘社编号:
分子量:
145.16 (anhydrous basis)
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
216-560-6
Beilstein/REAXYS Number:
5989589
MDL number:
Assay:
97%
Quality Level
assay
97%
mp
52-55 °C (lit.)
SMILES string
[H]O[H].[O-][n+]1cccc2ccccc12
InChI
1S/C9H7NO.H2O/c11-10-7-3-5-8-4-1-2-6-9(8)10;/h1-7H;1H2
InChI key
CUSWDTBBCIXCRB-UHFFFAOYSA-N
General description
Quinoline N-oxide hydrate forms complexes with lanthanide chloride.
Application
Quinoline N-oxide hydrate was used in quantitative determination of nitrones using trifluoroacetic anhydride-sodium iodide reagent.
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
此项目有
Lanthanide chloride complexes with quinoline-n-oxide.
Kingston JV, et al.
J. Inorg. Nucl. Chem., 31(10), 3181-3185 (1969)
The application of trifluoroacetic anhydride-sodium iodide (TFAA-I) system for quantitative determination of nitrones.
Clesielski W, et al.
Canadian Journal of Chemistry, 68(5), 679-684 (1990)
Oleg V Larionov et al.
Organic letters, 16(3), 864-867 (2014-01-15)
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 copper catalysis and activation by lithium fluoride or magnesium chloride. The utility of this method
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| T7140-1G | 04061835385089 |
| T7140-500MG | 04061838061294 |
| T7140-50G | 04061835385096 |
| T7140-5G | 04061837372308 |
| T7752-100ML | 04061837378591 |
| T7752-1L | 04061837378607 |
| 92860-10ML | 04061833270493 |
| 44895-U | 04061832312866 |
| 870110O-1MG | 04061835353712 |
| 92860-5ML | 04061833270509 |
| 41679-100MG | 04061832089867 |
| T7140-10G | 04061837372292 |
| Y0001113 | 04061837584077 |
| 122327-25G | 04061838721006 |
| 122327-5G | 04061838721020 |