Skip to Content
MilliporeSigma
All Photos(1)

Documents

183067

Sigma-Aldrich

6-Methoxyquinoline

98%

Synonym(s):

6-Methoxyquinoline

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C10H9NO
CAS Number:
5263-87-6
Molecular Weight:
159.18
Beilstein/REAXYS Number:
115244
EC Number:
226-077-2
MDL number:
MFCD00006800
UNSPSC Code:
12352100
PubChem Substance ID:
24851029
NACRES:
NA.22

assay

98%

refractive index

n20/D 1.625 (lit.)

bp

140-146 °C/15 mmHg (lit.)

mp

18-20 °C (lit.)

density

1.15 g/mL at 20 °C (lit.)

SMILES string

COc1ccc2ncccc2c1

InChI

1S/C10H9NO/c1-12-9-4-5-10-8(7-9)3-2-6-11-10/h2-7H,1H3

InChI key

HFDLDPJYCIEXJP-UHFFFAOYSA-N

Gene Information

human ... CYP2D6(1565)

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

6-Methoxyquinoline is used as a precursor in the synthesis of:
  • Fluorescent zinc and chlorine sensors.
  • 5-Amino-2-aroylquinolines as potent tubulin polymerization inhibitors.
  • 3-Fluoro-6-methoxyquinoline derivatives as inhibitors of bacterial DNA gyrase and topoisomerase.
  • Cobalt-based ternary metal-organic complex as single?ion magnets.

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H315,H319

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

>230.0 °F

flash_point_c

> 110 °C

ppe

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

5-Amino-2-aroylquinolines as highly potent tubulin polymerization inhibitors. Part 2. The impact of bridging groups at position C-2.
Lee H-Y, et al.
Journal of Medicinal Chemistry, 54(24), 8517-8525 (2011)
Roland J Reischl et al.
Journal of chromatography. A, 1269, 262-269 (2012-08-28)
The determination of trace amounts of d-amino acids (d-AAs) even in tissue samples of higher developed animals, mammals and humans has opened a wide field of biological questions to be investigated. d-Ala, d-Asp and d-Ser have already been identified to
Novel 3-fluoro-6-methoxyquinoline derivatives as inhibitors of bacterial DNA gyrase and topoisomerase IV.
Mitton-Fry MJ, et al.
Bioorganic & Medicinal Chemistry Letters, 27(15), 3353-3358 (2017)
Single-Ion Magnets Based on Mononuclear Cobalt (II) Complexes with Sulfadiazine.
Villa-Perez C, et al.
European Journal of Inorganic Chemistry, 2016(29), 4835-4841 (2016)
Richard G Painter et al.
Analytical chemistry, 78(9), 3133-3137 (2006-04-29)
Human neutrophils synthesize hypochlorous acid, a nonradical oxidant, as one of the antimicrobial agents to kill phagocytosed pathogens within phagolysosomes. The production of HOCl is catalyzed by myeloperoxidase using chloride anions (Cl-). Even though various approaches have been documented to
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service