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5548-72-1

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5548-72-1 Usage

Core structure

Quinoline-8-ol

Substituent

Hydroxyphenylimino group

Synthetic molecule

Yes

Therapeutic applications

+ Antioxidant properties
+ Metal chelating properties

Potential uses

+ Fluorescent chemosensors
+ Corrosion inhibitor in industrial applications

Versatility

Diverse potential applications in chemistry and biomedicine

Check Digit Verification of cas no

The CAS Registry Mumber 5548-72-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,4 and 8 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5548-72:
(6*5)+(5*5)+(4*4)+(3*8)+(2*7)+(1*2)=111
111 % 10 = 1
So 5548-72-1 is a valid CAS Registry Number.

5548-72-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(2-hydroxyanilino)methylidene]quinolin-8-one

1.2 Other means of identification

Product number -
Other names 8-Hydroxy-chinolin-2-carbaldehyd-2-hydroxyanil

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:5548-72-1 SDS

5548-72-1Downstream Products

5548-72-1Relevant articles and documents

Homoleptic CoII, NiII, CuII, and ZnII Complexes Based on 8-Hydroxylquinoline Schiff Base Derivative: a Combined Synthetic, Spectral, Structural, and Magnetic Study

González, Déborah,Arrué, Ramón,Matamala-Cea, Edison,Arancibia, Rodrigo,Hamon, Paul,Cador, Olivier,Roisnel, Thierry,Hamon, Jean-René,Novoa, Néstor

, p. 4720 - 4730 (2018/11/27)

A series of four new homoleptic CoII, NiII, CuII and ZnII complexes (1–4) of the type M(HL)2, where HL– stands for the deprotonated form of the tridentate O,N,N-donor Schiff base ligand obt

Antifungal properties of new series of quinoline derivatives

Musiol, Robert,Jampilek, Josef,Buchta, Vladimir,Silva, Luis,Niedbala, Halina,Podeszwa, Barbara,Palka, Anna,Majerz-Maniecka, Katarzyna,Oleksyn, Barbara,Polanski, Jaroslaw

, p. 3592 - 3598 (2007/10/03)

The series of quinoline derivatives were prepared. The synthetic approach, analytical, and spectroscopic data of all synthesized compounds are presented. All the prepared derivatives were analyzed using the reversed-phase high performance liquid chromatog

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