H57602
2-Methyl-8-quinolinol
98%
Synonym(s):
8-Hydroxyquinaldine
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100 G
$77.00
About This Item
Empirical Formula (Hill Notation):
C10H9NO
CAS Number:
Molecular Weight:
159.18
Beilstein/REAXYS Number:
119194
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
assay
98%
bp
267 °C (lit.)
mp
71-73 °C (lit.)
SMILES string
Cc1ccc2cccc(O)c2n1
InChI
1S/C10H9NO/c1-7-5-6-8-3-2-4-9(12)10(8)11-7/h2-6,12H,1H3
InChI key
NBYLBWHHTUWMER-UHFFFAOYSA-N
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Related Categories
General description
signalword
Warning
hcodes
pcodes
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1
Storage Class
11 - Combustible Solids
wgk_germany
WGK 2
flash_point_f
282.2 °F - closed cup
flash_point_c
139 °C - closed cup
ppe
Eyeshields, Gloves
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Monika Krawczyk et al.
Molecules (Basel, Switzerland), 25(18) (2020-09-17)
One of the main factors limiting the effectiveness of many drugs is the difficulty of their delivery to their target site in the cell and achieving the desired therapeutic dose. Moreover, the accumulation of the drug in healthy tissue can
J Thomas Leonard et al.
European journal of medicinal chemistry, 43(1), 81-92 (2007-04-25)
HIV-1 integrase inhibitory activity data of styrylquinoline derivatives have been subjected to 3D-QSAR study by molecular shape analysis (MSA) technique using Cerius(2) version 4.8 software (Accelrys). For the selection of test set compounds, initially a QSAR analysis was done based
Jakub Wantulok et al.
Molecules (Basel, Switzerland), 25(9) (2020-05-02)
A new approach to the synthesis of selected quinolinecarbaldehydes with carbonyl groups located at C5 and/or in C7 positions is presented in this paper in conjunction with spectroscopic characterization of the products. The classical Reimer-Tiemann, Vilsmeier-Haack and Duff aldehyde synthesis
Infrared Spectra, Density Functional Theory and Hartree-Fock Theoretical Calculations of 2-Methyl-8-quinolinol.
Arici K and Yilmaz R.
Asian Journal of Chemistry, 25(13), 7106-7106 (2013)
Kristiana T Santoso et al.
Bioorganic & medicinal chemistry, 27(16), 3532-3545 (2019-07-03)
A library of thirty-two quinolinequinones (QQs) with various amine substituents at the 6- and 7-positions were synthesised efficiently and in good yields for evaluation as potential anti-tuberculosis agents. Mycobacterium tuberculosis growth inhibition assays demonstrated that QQs bearing moderate length alkyl
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