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59953-98-9

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59953-98-9 Usage

General Description

3-Hydroxyquinoline N-oxide, also known as 3-Hydroxyquinoline-8-oxide or Quinoxaline N-oxide, is a chemical compound derived from quinoline. It is a yellow crystalline solid, soluble in organic solvents and water. 3-Hydroxyquinoline N-oxide has been used as a reagent in the synthesis of organic compounds and as an intermediate in the production of pharmaceuticals. It also has potential applications in the field of materials science, particularly as a building block for the construction of organic electronic devices. Additionally, 3-Hydroxyquinoline N-oxide has been studied for its antibacterial and antitumor properties, showing promising results in inhibiting the growth of certain bacteria and cancer cells.

Check Digit Verification of cas no

The CAS Registry Mumber 59953-98-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,9,5 and 3 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 59953-98:
(7*5)+(6*9)+(5*9)+(4*5)+(3*3)+(2*9)+(1*8)=189
189 % 10 = 9
So 59953-98-9 is a valid CAS Registry Number.

59953-98-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-oxidoquinolin-1-ium-3-ol

1.2 Other means of identification

Product number -
Other names 3-Quinolinol 1-oxide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:59953-98-9 SDS

59953-98-9Downstream Products

59953-98-9Relevant articles and documents

ELECTROPHILIC REACTIONS OF 3-HYDROXYQUINOLINE-1-OXIDE

Gol'tsova, L. V.,Lezina, V. P.,Kuz'min, V. I.,Smirnov, L. D.

, p. 1522 - 1524 (1984)

-

Synthesis of 8-Aminoquinolines by Using Carbamate Reagents: Facile Installation and Deprotection of Practical Amidating Groups

Gwon, Donghyeon,Hwang, Heejun,Kim, Hye Kyung,Marder, Seth R.,Chang, Sukbok

supporting information, p. 17200 - 17204 (2016/01/25)

Described herein is the development of practical routes to 8-aminoquinolines by using readily installable and easily deprotectable amidating reagents. Two scalable procedures were optimized under RhIII-catalyzed conditions: i) the use of pre-generated chlorocarbamates and ii) a two-step one-pot process that directly employs carbamates. Both approaches are highly convenient for the gram-scale synthesis of 8-aminoquinolines under mild conditions. Facile deprotection of the synthetically versatile amidating groups was achieved under the Pd-catalyzed transfer hydrogenation conditions with simultaneous deoxygenation of quinoline N-oxides, thus yielding 8-aminoquinolines in excellent overall efficiency.

KINETICS OF N-OXIDATION OF COMPOUNDS OF THE QUINOLINE SERIES AND ISOMERIC BENZOQUINOLINES BY PERBENZOIC ACID IN CHLOROFORM AND AQUEOUS DIOXANE

Lokhov, R. E.

, p. 72 - 76 (2007/10/02)

The kinetics of the N-oxidation with perbenzoic acid of 15 derivatives of quinoline and benzoquinoline in chloroform and 19 compounds in 50percent aqueous dioxane at 20, 25, 30, and 35 deg C were subjected to a comparative study.The rate constants, parameters of Arrhenius equation, and the activation energies for the N-oxidation of the indicated monoazines were determined.A scale of the reactivities of derivatives of the quinoline series and benzoquinolines was calculated within the framework of general perturbation theory.

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