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Merck

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:
Assay:
98%
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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

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.

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)].


pictograms

Environment

signalword

Warning

hcodes

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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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)
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