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H57602

Sigma-Aldrich

2-Methyl-8-quinolinol

98%

Synonym(s):

8-Hydroxyquinaldine

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About This Item

Empirical Formula (Hill Notation):
C10H9NO
CAS Number:
826-81-3
Molecular Weight:
159.18
Beilstein:
119194
EC Number:
212-562-6
MDL number:
MFCD00006765
UNSPSC Code:
12352100
PubChem Substance ID:
24895707
NACRES:
NA.22

Quality Level

100

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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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
GHS09

Signal Word

Warning

Hazard Statements

H410

Precautionary Statements

P273 - P391 - P501

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

282.2 °F - closed cup

Flash Point(C)

139 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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
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)
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)
New type of arrangement of rare-earth quinolinolate. Molecular structure of scandium 2-methyl-8-quinolinolate.
Katkova MA, et al.
Inorgorganica Chimica Acta, 362(4), 1393-1395 (2009)
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