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Merck
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Documenti

C47000

Sigma-Aldrich

5-Chloro-8-quinolinol

95%

Sinonimo/i:

5-Chloro-8-hydroxyquinoline

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About This Item

Formula empirica (notazione di Hill):
C9H6ClNO
Numero CAS:
130-16-5
Peso molecolare:
179.60
Beilstein:
5289
Numero CE:
204-978-1
Numero MDL:
MFCD00006788
Codice UNSPSC:
12352100
ID PubChem:
24892714
NACRES:
NA.22

Saggio

95%

Forma fisica

crystals

Punto di fusione

122-124 °C (lit.)

Stringa SMILE

Oc1ccc(Cl)c2cccnc12

InChI

1S/C9H6ClNO/c10-7-3-4-8(12)9-6(7)2-1-5-11-9/h1-5,12H
CTQMJYWDVABFRZ-UHFFFAOYSA-N

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Categorie correlate

Pittogrammi

Exclamation markEnvironment
GHS07,GHS09

Avvertenze

Warning

Indicazioni di pericolo

H302,H317,H319,H410

Classi di pericolo

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Skin Sens. 1

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

Certificati d'analisi (COA)

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8-hydroxy-quinoline-5-carbaldehyde AldrichCPR

Sigma-Aldrich

CDS018146

8-hydroxy-quinoline-5-carbaldehyde

8-Hydroxyquinoline ACS reagent, 98.5%

Sigma-Aldrich

252565

8-Hydroxyquinoline

V Arjunan et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 72(4), 783-788 (2008-12-30)
The Fourier transform infrared (FTIR) and FT-Raman spectra of 7-bromo-5-chloro-8-hydroxyquinoline (BCHQ) have been measured in the range 4000-400 and 4000-100cm(-1), respectively. Complete vibrational assignment and analysis of the fundamental modes of the compound were carried out using the observed FTIR
E J Wojtowicz
Journal of pharmaceutical sciences, 73(10), 1430-1433 (1984-10-01)
A reverse-phase high-performance liquid chromatographic (HPLC) method was developed for determining iodochlorhydroxyquin, 5,7-dichloro-8-hydroxyquinoline, and 5,7-diiodo-8-hydroxyquinoline in creams, ointments, shampoos, tablets, and bulk drugs. A column packed with 10-micron phenyl-silica and a mobile phase of 0.001 M NiCl2 in acetonitrile-methanol-water (30:20:50)
Poonpilas Hongmanee et al.
Antimicrobial agents and chemotherapy, 51(3), 1105-1106 (2006-12-21)
The in vitro activities of cloxyquin (5-chloroquinolin-8-ol) against 9 standard strains and 150 clinical isolates of Mycobacterium tuberculosis were studied. The MICs ranged from 0.062 to 0.25 microg/ml. The MIC(50) and MIC(90) were 0.125 and 0.25 microg/ml, respectively. These indicate
Oleg V Larionov et al.
Organic letters, 16(3), 864-867 (2014-01-15)
A one-step transformation of heterocyclic N-oxides to 2-alkyl-, aryl-, and alkenyl-substituted N-heterocycles is described. The success of this broad-scope methodology hinges on the combination of copper catalysis and activation by lithium fluoride or magnesium chloride. The utility of this method
Nikoleta Stoyanova et al.
Materials science & engineering. C, Materials for biological applications, 41, 119-126 (2014-06-09)
For the first time the preparation of defect-free fibers from immiscible blends of high molar mass poly(lactic acid) (PLA) and poly(butylene succinate) (PBS) in the whole range of the polyester weight ratios is shown. Electrospinning using the solvent-nonsolvent approach proved
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