Merck
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文件

A79205

Sigma-Aldrich

5-氨基喹啉

97%

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别名:
5-喹啉胺
经验公式（希尔记法）:
C9H8N2
CAS号:
611-34-7
分子量:
144.17
Beilstein:
114479
EC 号:
210-266-1
MDL编号:
MFCD00006797
PubChem化学物质编号:
24891293
NACRES:
NA.22

检测方案

97%

形式

powder

bp

310 °C (lit.)

mp

106-109 °C (lit.)

SMILES string

Nc1cccc2ncccc12

InChI

1S/C9H8N2/c10-8-4-1-5-9-7(8)3-2-6-11-9/h1-6H,10H2

InChI key

XMIAFAKRAAMSGX-UHFFFAOYSA-N

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相关类别

象形图

Exclamation mark
GHS07

警示用语：

Warning

危险声明

H315 - H319

危险分类

Eye Irrit. 2 - Skin Irrit. 2

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

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R Banoo et al.
Indian journal of biochemistry & biophysics, 30(4), 229-233 (1993-08-01)
In vitro oxidation and acetylation of 5-aminoquinoline by rabbit liver enzyme preparation has been investigated. Incubation of 5-aminoquinoline with cytosol fraction of the enzyme preparation in the presence of acetyl coenzyme-A gave rise to three different products, viz. 5-amino-2-hydroxy quinoline
V Arjunan et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 74(5), 1215-1223 (2009-10-27)
The Fourier transform infrared (FTIR) and FT-Raman spectra of 5-aminoquinoline (5AQ) have been recorded in the range 4000-400 and 3500-100 cm(-1), respectively. The complete vibrational assignment and analysis of the fundamental modes of the compounds were carried out using the
B G Siim et al.
Biochemical pharmacology, 48(8), 1593-1604 (1994-10-18)
The 4-alkylamino-5-nitroquinolines (5NQs) are a new series of bioreductive drugs that exhibit varying degrees of selective toxicity (up to 60-fold) under hypoxic conditions in cell culture. This study tested the hypothesis that differences in hypoxia-selective cytotoxicity in this series reflect
Jagat P Bridhkoti et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 79(3), 412-417 (2011-04-20)
Photophysical properties of 5-aminoquinoline (5AQ) have been investigated in various non-polar and polar (protic and aprotic) solvents using steady state and time resolved fluorescence. In aprotic solvents, the spectral maxima depend on the polarity. However, in protic solvents both the
Maria Sittig et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 27(3), 1072-1079 (2020-09-29)
Quinoline photobases exhibit a distinctly higher pKa in their electronically excited state than in the ground state, thereby enabling light-controlled proton transfer reactions, for example, in molecular catalysis. The absorption of UV light translates to a pKa jump of approximately
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