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Merck
CN

145025

5-氨基-6-硝基喹啉

97%

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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
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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.


pictograms

Exclamation mark

signalword

Warning

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



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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
145025-5G04061838736079