N24005
6-硝基喹啉
98%
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关于此项目
经验公式（希尔记法）:
C9H6N2O2
化学文摘社编号:
分子量:
174.16
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
210-346-6
MDL number:
Assay:
98%
Form:
powder
InChI
1S/C9H6N2O2/c12-11(13)8-3-4-9-7(6-8)2-1-5-10-9/h1-6H
InChI key
SMHPLBXIVNQFBA-UHFFFAOYSA-N
SMILES string
[O-][N+](=O)c1ccc2ncccc2c1
assay
98%
form
powder
mp
151-153 °C (lit.)
Quality Level
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Carc. 2
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
法规信息
新产品
此项目有
Fanny Widjaja et al.
Journal of the American Society for Mass Spectrometry, 28(7), 1392-1405 (2017-05-01)
The gas-phase reactivity of two aromatic carbon-centered σ,σ-biradicals (meta-benzyne analogs) and a related monoradical towards small oligonucleotides of differing lengths was investigated in a Fourier-transform ion cyclotron resonance (FT-ICR) mass spectrometer coupled with laser-induced acoustic desorption (LIAD). The mono- and
Xiulong Shen et al.
Chemical research in toxicology, 32(3), 348-361 (2019-03-01)
Enzymatic one-electron reduction of heterocyclic N-oxides can lead to the intracellular generation of reactive oxygen species via several different chemical pathways. These reactions may be relevant to hypoxia-selective anticancer drugs, antimicrobial agents, and unwanted toxicity of heterocylic nitrogen compounds.
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