H57602
2-Methyl-8-quinolinol
98%
Synonym(s):
8-Hydroxyquinaldine
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About This Item
Empirical Formula (Hill Notation):
C10H9NO
CAS Number:
Molecular Weight:
159.18
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
212-562-6
Beilstein/REAXYS Number:
119194
MDL number:
Product Name
2-Methyl-8-quinolinol, 98%
Quality Level
InChI key
NBYLBWHHTUWMER-UHFFFAOYSA-N
InChI
1S/C10H9NO/c1-7-5-6-8-3-2-4-9(12)10(8)11-7/h2-6,12H,1H3
SMILES string
Cc1ccc2cccc(O)c2n1
assay
98%
bp
267 °C (lit.)
mp
71-73 °C (lit.)
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Application
2-Methyl-8-quinolinol (HqMe) may be used as a ligand for preparing bis (2-methyl-8-quinolinolato) aluminum(III)-μ-oxo-bis (2-methyl-8-quinolinolato ) aluminum (III). It may also be used in the preparation of a scandium 2-methyl-8-quinolinolate complex [Sc(qMe)4(H)].
General description
2-Methyl-8-quinolinol is a methyl substituted quinolinol derivative that shows fungicidal property. It can also undergo complexation with transition metal complexes.
signalword
Warning
hcodes
pcodes
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1
Storage Class
11 - Combustible Solids
wgk
WGK 2
flash_point_f
282.2 °F - closed cup
flash_point_c
139 °C - closed cup
ppe
Eyeshields, Gloves
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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
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
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)
Antifungal activity of 5-,7-, and 5,7-substituted 2-methyl-8-quinolinols.
Gershon H, et al.
Antimicrobial Agents and Chemotherapy, 1(5), 373-375 (1972)
The crystal and molecular structure of bis-(2-methyl-8-quinolinolato) oxovanadium (IV).
Shiro M and Fernando Q.
Journal of the Chemical Society. Chemical Communications, 1, 63-64 (1971)
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