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3-(7-Chloro-quinoline-4-yl)-furan is a heterocyclic chemical compound characterized by the fusion of a furan ring with a 7-chloro-quinoline-4-yl group. 3-(7-CHLORO-QUINOLINE-4-YL)-FURAN exhibits potential pharmaceutical applications, particularly in the realms of antimicrobial and antimalarial treatments. The incorporation of a chloro group in its structure is likely to augment its biological activity, facilitating interactions with biological targets and enhancing its efficacy.

179380-95-1

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179380-95-1 Usage

Uses

Used in Pharmaceutical Industry:
3-(7-CHLORO-QUINOLINE-4-YL)-FURAN is used as an antimicrobial agent for its ability to inhibit the growth of various microorganisms, which makes it a valuable component in the development of new antibiotics to combat drug-resistant infections.
Used in Antimalarial Applications:
In the field of antimalarial drug development, 3-(7-CHLORO-QUINOLINE-4-YL)-FURAN is utilized for its potential to treat malaria, a disease caused by parasites that are becoming increasingly resistant to existing treatments. Its unique structure and pharmacological properties offer a new avenue for the creation of effective antimalarial medications.
Used in Medicinal Chemistry Research:
3-(7-CHLORO-QUINOLINE-4-YL)-FURAN serves as a key compound in medicinal chemistry for further research and development. Its unique structure and potential to interact with biological targets make it a promising candidate for the design of new drugs with improved efficacy and selectivity.
Used in Drug Development:
In the drug development sector, 3-(7-CHLORO-QUINOLINE-4-YL)-FURAN is employed as a lead compound for the synthesis of novel pharmaceuticals. Its potential to inhibit the growth of microorganisms and parasites positions it as a valuable asset in the creation of new therapeutic agents to address unmet medical needs.

Check Digit Verification of cas no

The CAS Registry Mumber 179380-95-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,9,3,8 and 0 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 179380-95:
(8*1)+(7*7)+(6*9)+(5*3)+(4*8)+(3*0)+(2*9)+(1*5)=181
181 % 10 = 1
So 179380-95-1 is a valid CAS Registry Number.

179380-95-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-chloro-4-(furan-3-yl)quinoline

1.2 Other means of identification

Product number -
Other names 4-(3-furyl)-7-chloroquinoline

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:179380-95-1 SDS

179380-95-1Downstream Products

179380-95-1Relevant academic research and scientific papers

Quinolines as potent 5-lipoxygenase inhibitors: Synthesis and biological profile of L-746,530

Dube, Daniel,Blouin, Marc,Brideau, Christine,Chan, Chi-Chung,Desmarais, Sylvie,Ethier, Diane,Falgueyret, Jean-Pierre,Friesen, Richard W.,Girard, Mario,Girard, Yves,Guay, Jocelyne,Riendeau, Denis,Tagari, Philip,Young, Robert N.

, p. 1255 - 1260 (2007/10/03)

Leukotriene biosynthesis inhibitors have potential as new therapeutic agents for asthma and inflammatory diseases. A series of novel substituted 2- cyanoquinolines have been synthesized and the structure activity relationships were evaluated with respect

Bis (biaryl) compounds as inhibitors of leukotriene biosynthesis

-

, (2008/06/13)

Compounds having the Formula I: STR1 are inhibitors of leukotriene biosynthesis. These compounds are useful as anti-asthmatic, anti-allergic, anti-inflammatory, and cytoprotective agents. They are also useful in treating angina, cerebral spasm, glomerular nephritis, hepatitis, endotoxemia, uveitis, and allograft rejection and in preventing the formation of atherosclerotic plaques.

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