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Ethyl 5-hydroxyquinoline-3-carboxylate is a chemical compound with the molecular formula C13H11NO3. It is a derivative of quinoline, and its structure contains a hydroxy and an ethyl ester group attached to the quinoline ring.
Used in Pharmaceutical Industry:
Ethyl 5-hydroxyquinoline-3-carboxylate is used as a building block for the synthesis of various pharmacologically active substances. Its quinoline scaffold has been studied for its antitumor and antimicrobial activities.
Used in Antioxidant Applications:
Ethyl 5-hydroxyquinoline-3-carboxylate is used as an antioxidant and free radical scavenger, making it potentially useful in the development of drugs targeting oxidative stress-related diseases.
Used in Analytical Chemistry and Bioimaging:
Ethyl 5-hydroxyquinoline-3-carboxylate is used as a fluorescent probe for metal ions in analytical chemistry and bioimaging.

911108-83-3

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911108-83-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 911108-83-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,1,1,0 and 8 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 911108-83:
(8*9)+(7*1)+(6*1)+(5*1)+(4*0)+(3*8)+(2*8)+(1*3)=133
133 % 10 = 3
So 911108-83-3 is a valid CAS Registry Number.

911108-83-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 5-oxo-1H-quinoline-3-carboxylate

1.2 Other means of identification

Product number -
Other names ETHYL 5-HYDROXYQUINOLINE-3-CARBOXYLATE

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:911108-83-3 SDS

911108-83-3Relevant academic research and scientific papers

Rational design of central selective acetylcholinesterase inhibitors by means of a "bio-oxidisable prodrug" strategy

Bohn, Pierre,Le Fur, Nicolas,Hagues, Guillaume,Costentin, Jean,Torquet, Nicolas,Papamicael, Cyril,Marsais, Francis,Levacher, Vincent

experimental part, p. 2612 - 2618 (2009/10/30)

This work deals with the design of a "bio-oxidisable prodrug" strategy for the development of new central selective acetylcholinesterase inhibitors. This prodrug approach is expected to reduce peripheral anticholinesterase activity responsible for various

NEW HETEROCYCLIC COMPOUNDS, THEIR PREPARATION AND THEIR USE AS MEDICAMENTS, IN PARTICULAR AS ANTI-ALZHEIMER AGENTS

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Page/Page column 45, (2008/06/13)

The invention is related to compound which comprises at least one radical C=Y, Y being O or S, and an oxidable and non protonable nitrogen atom N wherein the distance (d) between the at least one carbon atom of the radical group C=Y and the nitrogen atom, when oxidized, is comprised between 0.3 and 0.8 nanometers. The invention is related to new heterocyclic compounds defined by formula G, their preparation, to pharmaceutical compositions comprising them and to their use as therapeutic agents, particularly in the treatment of neurodegenerative or Alzheimer disease.

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