ProphetesAI is thinking...
hydroxyquinoline
MindMap
Loading...
Sources
hydroxyquinoline
hydroxyquinoline Chem. (haɪˌdrɒksɪˈkwɪnəliːn) [f. hydroxy- + quinoline.] Any of the seven monohydroxy derivatives, C9H7NO, of quinoline, esp. oxine (8-hydroxyquinoline).1881 Jrnl. Chem. Soc. XL. 613 An excellent yield of hydroxyquinoline is obtained by fusing the sulphonic acid with three times its ...
Oxford English Dictionary
prophetes.ai
8-Hydroxyquinoline
8-Hydroxyquinoline (also known as oxine) is an organic compound derived from the heterocycle quinoline. In aqueous solution 8-hydroxyquinoline has a pKa value of ca. 9.9 It reacts with metal ions, losing the proton and forming 8-hydroxyquinolinato-chelate
wikipedia.org
en.wikipedia.org
2-hydroxyquinoline 8-monooxygenase
In enzymology, a 2-hydroxyquinoline 8-monooxygenase () is an enzyme that catalyzes the chemical reaction
quinolin-2-ol + NADH + H+ + O2 quinolin-2,8-
wikipedia.org
en.wikipedia.org
4-hydroxyquinoline 3-monooxygenase
In enzymology, a 4-hydroxyquinoline 3-monooxygenase () is an enzyme that catalyzes the chemical reaction
quinolin-4-ol + NADH + H+ + O2 quinolin-3,4-
wikipedia.org
en.wikipedia.org
oxine
oxine Chem. (ˈɒksiːn) [ad. G. oxin (Hahn & Vieweg 1927, in Zeitschr. f. anal. Chem. LXXI. 123), f. oxychinolin, hydroxyquinoline.] 8-Hydroxyquinoline, C9H7NO, a crystalline phenol which forms water-insoluble complexes with many metal ions and is used in analysis and as a deodorant and antibacterial ...
Oxford English Dictionary
prophetes.ai
2-hydroxyquinoline 5,6-dioxygenase
In enzymology, a 2-hydroxyquinoline 5,6-dioxygenase () is an enzyme that catalyzes the chemical reaction
quinolin-2-ol + NADH + H+ + O2 2,5,6-trihydroxy
wikipedia.org
en.wikipedia.org
Clamoxyquine
Thus, Mannich condensation of the hydroxyquinoline (1) with formaldehyde and N,N-diethylpropylenediamine affords clamoxyquin (2).
wikipedia.org
en.wikipedia.org
Chlorquinaldol
It is a chlorinated derivative of the popular chelating agent 8-hydroxyquinoline. It is applied topically as a cream and internally as a losenge.
wikipedia.org
en.wikipedia.org
C9H7NO
{{DISPLAYTITLE:C9H7NO}}
The molecular formula C9H7NO (molar mass: 145.16 g/mol, exact mass: 145.0528 u) may refer to:
8-Hydroxyquinoline
Indole-3-carboxaldehyde
wikipedia.org
en.wikipedia.org
Tris(8-hydroxyquinolinato)aluminium
Widely abbreviated Alq3, it is a coordination complex wherein aluminium is bonded in a bidentate manner to the conjugate base of three 8-hydroxyquinoline Synthesis
The compound is prepared by the reaction of 8-hydroxyquinoline with aluminium(III) sources
Al3+ + 3 C9H7NO → Al(C9H6NO)3 + 3 H+
Applications
wikipedia.org
en.wikipedia.org
Thulium acetylacetonate
The acetonitrile solution of its dihydrate and the dichloromethane solution of 5-[(4-fluorobenzylidene)amino]-8-hydroxyquinoline (HL) react by heating
wikipedia.org
en.wikipedia.org
Terbium acetylacetonate
of ammonia, acetylacetone and terbium nitrate:
3 NH3 + 3 Hacac + Tb(NO3)3 → Tb(acac)3 + 3 NH4NO3
It reacts with 5-[(2-thiophene methylene)amino]-8-hydroxyquinoline
wikipedia.org
en.wikipedia.org
8-Mercaptoquinoline
The compound is an analog of 8-hydroxyquinoline, a common chelating agent. The compound is a colorless solid.
wikipedia.org
en.wikipedia.org
Niementowski quinoline synthesis
The Niementowski quinoline synthesis is the chemical reaction of anthranilic acids and ketones (or aldehydes) to form γ-hydroxyquinoline derivatives. Overview
In 1894, Niementowski reported that 2-phenyl-4-hydroxyquinoline was formed when anthranilic acid and acetophenone were heated to 120–130 °C.
wikipedia.org
en.wikipedia.org
Knorr quinoline synthesis
For instance, the compound benzoylacetanilide (1) forms the 2-hydroxyquinoline (2) in a large excess of polyphosphoric acid (PPA) but 4-hydroxyquinoline Aniline reacts with another equivalent of benzoylacetanilide before forming the 4-hydroxyquinoline.
wikipedia.org
en.wikipedia.org