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H6878

Sigma-Aldrich

8-Hydroxychinolin

Synonym(e):

8-Hydroxychinolin, 8-Chinolinol, 8-Oxychinolin, Oxin

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About This Item

Empirische Formel (Hill-System):
C9H7NO
CAS-Nummer:
148-24-3
Molekulargewicht:
145.16
Beilstein:
114512
EG-Nummer:
205-711-1
MDL-Nummer:
MFCD00006807
UNSPSC-Code:
12352005
PubChem Substanz-ID:
24895771
NACRES:
NA.21

Assay

≥98.5%

Qualitätsniveau

200

Form

powder

mp (Schmelzpunkt)

72.5-74.0 °C

Wirkungsspektrum von Antibiotika

fungi

Wirkungsweise

DNA synthesis | interferes
enzyme | inhibits

SMILES String

Oc1cccc2cccnc12

InChI

1S/C9H7NO/c11-8-5-1-3-7-4-2-6-10-9(7)8/h1-6,11H

InChIKey

MCJGNVYPOGVAJF-UHFFFAOYSA-N

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Allgemeine Beschreibung

Chemical structure: quinolone

Anwendung

Used as a lipophilic monoprotic bidentate chelating agent.

Signalwort

Danger

Gefahreneinstufungen

Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Repr. 1B - Skin Sens. 1

Lagerklassenschlüssel

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

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Analysenzertifikate (COA)

Lot/Batch Number
0000362693
0000362694
0000362695
0000322543
0000322542

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8-Hydroxychinolin-β-D-glucuronid Natriumsalz ≥98.0% (HPLC)

Sigma-Aldrich

38153

8-Hydroxychinolin-β-D-glucuronid Natriumsalz

5,7-Dichlor-8-Chinolinol 99%

Sigma-Aldrich

D64600

5,7-Dichlor-8-Chinolinol

Pawel Strzelczyk et al.
Scientific reports, 10(1), 17516-17516 (2020-10-17)
The mechanism of catalysis by the L-glutaminase-asparaginase from Pseudomonas 7A (PGA) was investigated using structural, mass spectrometry, and kinetic data. We had previously proposed mechanism of hydrolysis of L-Asn by the type II L-asparaginase from E. coli (EcAII), but that
María Isabel Fernández-Bachiller et al.
Journal of medicinal chemistry, 53(13), 4927-4937 (2010-06-16)
Tacrine and PBT2 (an 8-hydroxyquinoline derivative) are well-known drugs that inhibit cholinesterases and decrease beta-amyloid (Abeta) levels by complexation of redox-active metals, respectively. In this work, novel tacrine-8-hydroxyquinoline hybrids have been designed, synthesized, and evaluated as potential multifunctional drugs for
David M Rubush et al.
Journal of the American Chemical Society, 134(33), 13554-13557 (2012-08-09)
The desymmetrization of p-peroxyquinols using a Brønsted acid-catalyzed acetalization/oxa-Michael cascade was achieved in high yields and selectivities for a variety of aliphatic and aryl aldehydes. Mechanistic studies suggest that the reaction proceeds through a dynamic kinetic resolution of the peroxy
Bhimashankar Mitkari et al.
Experimental neurology, 239, 158-162 (2012-10-13)
Cell therapies from various sources have been under intense research in stroke. Efficient homing of the cells to the injured brain without complications is necessary to realize the therapeutic potential of cell therapy. Intra-arterial (IA) infusion of cells bypasses the
Steve Comby et al.
Inorganic chemistry, 51(19), 10158-10168 (2012-09-15)
A novel near-infrared (NIR) emissive lanthanide-based zinc sensor was designed, based on the self-assembly in aqueous solution between the nonemissive coordinatively unsaturated Yb(III) cyclen complex 2·Yb and the sulfonated 8-hydroxyquinoline (8-HQS) chromophore, which was employed as a sensitizing antenna. The
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