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5,6,7-trichloroquinolin-8-ol is a chemical compound belonging to the quinolines class, characterized by the presence of three chlorine atoms at positions 5, 6, and 7, and a hydroxyl group at position 8. This heterocyclic compound is known for its potential applications in pharmaceuticals and agrochemicals, particularly as an intermediate in the synthesis of various bioactive molecules. Its chemical structure contributes to its reactivity and stability, making it a valuable component in the development of new drugs and pesticides.

5541-71-9

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5541-71-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5541-71-9 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 1 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5541-71:
(6*5)+(5*5)+(4*4)+(3*1)+(2*7)+(1*1)=89
89 % 10 = 9
So 5541-71-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H4Cl3NO/c10-5-4-2-1-3-13-8(4)9(14)7(12)6(5)11/h1-3,14H

5541-71-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,6,7-trichloroquinolin-8-ol

1.2 Other means of identification

Product number -
Other names 5,6,7-Trichlor-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:5541-71-9 SDS

5541-71-9Downstream Products

5541-71-9Relevant academic research and scientific papers

Preparation and fungitoxicity of some trichloro-, tribromo-, tetrachloro-, and tetrabromo-8-quinolinols

Gershon,Clarke,Gershon

, p. 1075 - 1080 (2001)

3,5,6-, 3,5,7-, 4,5,7-, and 5,6,7-trichloro- and -tribromo-8-quinolinols as well as 3,5,6,7-tetrachloro- and -tetrabromo-8-quinolinols were prepared and tested against six fungi (Aspergillus niger, Aspergillus oryzae, Myrothecium verrucaria, Trichoderma viride, Mucor cirinelloides, and Trichophyton mentagrophytes) in Sabouraud dextrose broth. The compounds strongly inhibit five fungi but not M. cirinelloides. They are less active than the related dichloro-8-quinolinols which is attributed to steric hindrance.

Preparation and fungitoxicity of some dichloro-8-quinolinols

Gershon, Herman,Clarke, Donald D.,Gershon, Muriel

, p. 653 - 659 (1999)

2,5-, 3,5-, 3,7-, 4,5-, 5,6-, und 6,7-Dichloro-8-quinolinols were prepared and tested along with their 3,6-and 5,7-analogues against six fungi (Aspergillus niger, A. oryzae, Myrothecium verrucaria, Trichoderma viride, Mucor cirinelloides, and Trichophyton mentagrophytes) in Sabouraud dextrose broth. Most of the compounds were strongly antifungal, inhibiting five of the fungi below 1 μg/ml. This activity is attributed to intramolecular synergism. M. cirinelloides was inhibited less by these compounds.

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