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关于此项目
经验公式(希尔记法):
C9H7N3O2
化学文摘社编号:
分子量:
189.17
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
252-822-6
MDL number:
Assay:
97%
Form:
powder
Quality Level
assay
97%
form
powder
mp
272-273 °C (dec.) (lit.)
functional group
nitro
SMILES string
Nc1c(ccc2ncccc12)[N+]([O-])=O
InChI
1S/C9H7N3O2/c10-9-6-2-1-5-11-7(6)3-4-8(9)12(13)14/h1-5H,10H2
InChI key
TYBYHEXFKFLRFT-UHFFFAOYSA-N
General description
Electrochemical reduction of 5-amino-6-nitroquinoline has been studied at carbon paste electrode by differential pulse voltammetry, direct current voltammetry, adsorptive stripping voltammetry and HPLC with electrochemical detection.
Application
5-Amino-6-nitroquinoline was used in preparation of imidazoquinoline derivatives.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Determination of 5-amino-6-nitroquinoline at a carbon paste electrode.
Nemcova L, et al.
Collection of Czechoslovak Chemical Communications, 74(10), 1477-1488 (2009)
J H Weisburger et al.
Environmental health perspectives, 67, 121-127 (1986-08-01)
Because mutagens typified by 2-amino-3-methylimidazo[4,5-f]quinoline (IQ) observed in cooked foods are widely consumed, detailed studies of their biochemical and biological properties including carcinogenicity are most important. IQ induces unscheduled DNA synthesis in liver cells, which when taken together with its
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 145025-5G | 04061838736079 |
