A79205
5-氨基喹啉
97%
别名:
5-喹啉胺
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关于此项目
经验公式（希尔记法）:
C9H8N2
化学文摘社编号:
分子量:
144.17
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-266-1
Beilstein/REAXYS Number:
114479
MDL number:
Assay:
97%
Form:
powder
产品名称
5-氨基喹啉, 97%
Quality Level
InChI key
XMIAFAKRAAMSGX-UHFFFAOYSA-N
InChI
1S/C9H8N2/c10-8-4-1-5-9-7(8)3-2-6-11-9/h1-6H,10H2
SMILES string
Nc1cccc2ncccc12
assay
97%
form
powder
bp
310 °C (lit.)
mp
106-109 °C (lit.)
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signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2
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
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
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
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
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
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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