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5,7-DICHLORO-4-HYDROXY-2-(TRIFLUOROMETHYL)QUINOLINE is a quinoline derivative with the molecular formula C11H5Cl2F3NO. It is a chemical compound that serves as an intermediate in the synthesis of pharmaceuticals and agrochemicals, known for its strong antimicrobial and antifungal properties. 5,7-DICHLORO-4-HYDROXY-2-(TRIFLUOROMETHYL)QUINOLINE is also utilized as a building block in organic synthesis, particularly for the production of fluorinated compounds, and has potential applications in materials science for the development of fluorescent dyes and optical materials.

59108-13-3

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59108-13-3 Usage

Uses

Used in Pharmaceutical Industry:
5,7-DICHLORO-4-HYDROXY-2-(TRIFLUOROMETHYL)QUINOLINE is used as a key intermediate in the synthesis of various pharmaceuticals for its antimicrobial and antifungal properties, contributing to the development of new drugs that combat resistant infections.
Used in Agrochemical Industry:
In the agrochemical sector, 5,7-DICHLORO-4-HYDROXY-2-(TRIFLUOROMETHYL)QUINOLINE is used as a component in the formulation of agricultural pesticides, leveraging its strong antimicrobial and antifungal properties to protect crops from diseases and pests.
Used in Organic Synthesis:
5,7-DICHLORO-4-HYDROXY-2-(TRIFLUOROMETHYL)QUINOLINE is used as a building block in organic synthesis, particularly for the production of fluorinated compounds, which have a wide range of applications in various chemical and pharmaceutical processes.
Used in Materials Science:
In the field of materials science, 5,7-DICHLORO-4-HYDROXY-2-(TRIFLUOROMETHYL)QUINOLINE is used for the development of novel fluorescent dyes and optical materials, taking advantage of its unique chemical structure and properties to create innovative materials with specific optical characteristics.

Check Digit Verification of cas no

The CAS Registry Mumber 59108-13-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,1,0 and 8 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 59108-13:
(7*5)+(6*9)+(5*1)+(4*0)+(3*8)+(2*1)+(1*3)=123
123 % 10 = 3
So 59108-13-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H4BrFO/c8-7-3-6(9)2-1-5(7)4-10/h1-4H

59108-13-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,7-Dichloro-4-hydroxy-2-(trifluoromethyl)quinoline

1.2 Other means of identification

Product number -
Other names 5,7-dichloro-2-(trifluoromethyl)-1H-quinolin-4-one

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:59108-13-3 SDS

59108-13-3Downstream Products

59108-13-3Relevant academic research and scientific papers

Structure-Activity relationships for a series of quinoline-based compounds active against replicating and nonreplicating mycobacterium tuberculosis

Lilienkampf, Annamaria,Jialin, Mao,Baojie, Wan,Yuehong, Wang,Franzblau, Scott G.,Kozikowski, Alan P.

supporting information; experimental part, p. 2109 - 2118 (2009/12/31)

Tuberculosis (TB) remains as a global pandemic that is aggravated by a lack of health care, the spread of HIV, and the emergence of multidrug-resistant TB (MDR-TB) and extensively drug-resistant TB (XDRTB) strains. New anti-TB drugs are urgently required to shorten the long 6-12 month treatment regimen and to battle drug-resistant Mtb strains. We have identified several potent quinoline-based anti-TB compounds, bearing an isoxazole containing side-chain. The most potent compounds, 7g and 13, exhibited submicromolar activity against the replicating bacteria (R-TB), with minimum inhibitory concentrations (MICs) of 0.77 and 0.95 μM, respectively. In general, these compounds also had micromolar activity against the nonreplicating persistent bacteria (NRP-TB) and did not show toxicity on Vero cells up to 128 μM concentration. Compounds 7g and 13 were shown to retain their anti-TB activity against rifampin, isoniazid, and streptomycin resistant Mtb strains. The results suggest that quinoline-isoxazole-based anti-TB compounds are promising leads for new TB drug development.

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