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5-iodo-8-quinolinol, commonly known as iodoquinol, is a chemical compound with antiprotozoal and amoebicide properties. It is an essential medicine used to treat infections caused by protozoa and other parasitic organisms. 5-iodo-8-quinolinol works by disrupting the energy production of these organisms, leading to their death. It is particularly effective against amoebiasis, an intestinal infection caused by the parasite Entamoeba histolytica. 5-iodo-8-quinolinol is typically administered orally and is well-tolerated, with common side effects including mild gastrointestinal symptoms. It is recognized by the World Health Organization as an essential medicine and is listed on its Model List of Essential Medicines, as well as in various national essential medicines lists for its effectiveness in treating parasitic infections.

13207-63-1

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13207-63-1 Usage

Uses

Used in Pharmaceutical Industry:
5-iodo-8-quinolinol is used as an antiprotozoal and amoebicide medication for the treatment of infections caused by protozoa and other parasitic organisms. It is particularly effective against amoebiasis, an intestinal infection caused by the parasite Entamoeba histolytica.
Used in Public Health:
5-iodo-8-quinolinol is used as an essential medicine by the World Health Organization and is listed on its Model List of Essential Medicines. It is recognized for its effectiveness in treating parasitic infections and is included in various national essential medicines lists, contributing to public health efforts to combat these infections.
Used in Medical Treatment:
5-iodo-8-quinolinol is used as a therapeutic agent in the treatment of patients suffering from infections caused by protozoa and other parasitic organisms. Its effectiveness in treating amoebiasis makes it a valuable component in the medical arsenal against such infections.
Used in Research and Development:
5-iodo-8-quinolinol serves as a subject of research and development in the field of pharmaceuticals and medicine. Its mechanism of action and potential applications in treating other parasitic infections are areas of ongoing study, with the aim of expanding its use and improving treatment options for patients.
Used in Drug Formulation:
5-iodo-8-quinolinol is used in the formulation of various pharmaceutical products, such as tablets and oral solutions, for the treatment of protozoal and parasitic infections. Its well-tolerated nature and effectiveness make it a suitable component in these formulations, ensuring patient compliance and therapeutic success.

Check Digit Verification of cas no

The CAS Registry Mumber 13207-63-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,0 and 7 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 13207-63:
(7*1)+(6*3)+(5*2)+(4*0)+(3*7)+(2*6)+(1*3)=71
71 % 10 = 1
So 13207-63-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H6INO/c10-7-3-4-8(12)9-6(7)2-1-5-11-9/h1-5,12H

13207-63-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-iodoquinolin-8-ol

1.2 Other means of identification

Product number -
Other names 5-Jod-chinolin-8-ol

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:13207-63-1 SDS

13207-63-1Relevant academic research and scientific papers

PURIFICATION TAGS OF SYNTHETIC PEPTIDES AND PROTEINS

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Paragraph 0041; 0042, (2013/08/28)

The present invention relates to a series of compounds useful for effecting purification, in particular for use in purification of synthetic peptides and proteins. The compounds of the invention are particularly efficient at securely anchoring peptides or

Palladium-catalysed reactions of 8-hydroxy- and 8-benzyloxy-5,7- diiodoquinoline under aminocarbonylation conditions

Takács, Attila,Szilágyi, Antal,ács, Péter,Márk, László,Peixoto, Andreia F.,Pereira, Mariette M.,Kollár, László

experimental part, p. 2402 - 2406 (2011/04/26)

Various 5-carboxamido-7-iodo-8-benzyloxyquinolines were synthesised via selective aminocarbonylation of 5,7-diiodo-8-benzyloxyquinoline in the presence of 'in situ' generated palladium(0) catalysts. Under similar conditions (50 °C, 80 bar CO), 5,7-bis(N-tert-butyl-glyoxylamido)-8-hydroxyquinoline was obtained using tert-butylamine as N-nucleophile. The unprotected 5,7-diiodo-8-hydroxyquinoline underwent dehydroiodination resulting in 8-hydroxyquinoline as the major product.

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