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3-Amino-7-chloro-3,4-dihydro-1H-quinolin-2-one is a condensed heterocyclic chemical compound characterized by a quinolin-2-one core, an amino group, and a chloro substituent. With the molecular formula C9H8ClN3O, 3-Amino-7-chloro-3,4-dihydro-1H-quinolin-2-one has garnered interest for its potential medicinal properties, particularly in antimicrobial and antifungal activities. It is also considered a promising candidate for the development of novel pharmaceuticals, such as antibacterial and antiviral agents, and has been explored for its potential in creating new materials with specific applications.

56433-13-7

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56433-13-7 Usage

Uses

Used in Pharmaceutical Development:
3-Amino-7-chloro-3,4-dihydro-1H-quinolin-2-one is used as a precursor in the synthesis of new pharmaceuticals for its antimicrobial and antifungal properties. It serves as a key component in the development of novel antibacterial and antiviral agents, contributing to the fight against drug-resistant infections.
Used in Material Science:
In the field of material science, 3-Amino-7-chloro-3,4-dihydro-1H-quinolin-2-one is utilized as a building block for the creation of new materials with unique properties. Its chemical structure allows for the engineering of materials with specific characteristics, such as enhanced stability or reactivity, for various applications.
Used in Antimicrobial Applications:
3-Amino-7-chloro-3,4-dihydro-1H-quinolin-2-one is employed as an antimicrobial agent, particularly effective against a range of bacteria and fungi. Its activity is attributed to its ability to disrupt essential cellular processes in microorganisms, thereby inhibiting their growth and proliferation.
Used in Antifungal Applications:
3-Amino-7-chloro-3,4-dihydro-1H-quinolin-2-one is also used as an antifungal agent, targeting various fungal species and preventing their growth. Its application in antifungal formulations can help in controlling fungal infections and maintaining the integrity of materials susceptible to fungal degradation.
Used in Research and Development:
3-Amino-7-chloro-3,4-dihydro-1H-quinolin-2-one serves as a subject of research for its potential applications in various industries. Its unique chemical properties make it an interesting candidate for further exploration and development, with the aim of discovering new uses and enhancing existing ones.

Check Digit Verification of cas no

The CAS Registry Mumber 56433-13-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,4,3 and 3 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 56433-13:
(7*5)+(6*6)+(5*4)+(4*3)+(3*3)+(2*1)+(1*3)=117
117 % 10 = 7
So 56433-13-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H9ClN2O/c10-6-2-1-5-3-7(11)9(13)12-8(5)4-6/h1-2,4,7H,3,11H2,(H,12,13)

56433-13-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-AMINO-7-CHLORO-3,4-DIHYDRO-1H-QUINOLIN-2-ONE

1.2 Other means of identification

Product number -
Other names 7-Chlor-3-amino-3,4-dihydro-carbostyril

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:56433-13-7 SDS

56433-13-7Downstream Products

56433-13-7Relevant academic research and scientific papers

PYRROLOPYRIDINE-2-CARBOXYLIC ACID AMIDES

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Page/Page column 26, (2008/06/13)

Compounds represented by Formula (I) or pharmaceutically acceptable salts thereof, are useful in the prophylactic or therapeutic treatment of diabetes, hyperglycemia, hypercholesterolemia, hyperinsulinemia, hyperlipidemia, hypertension, atherosclerosis or tissue ischemia e.g. myocardial ischemia, and as cardioprotectants.

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