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ETHYL 4-HYDROXY-6-(TRIFLUOROMETHOXY)QUINOLINE-3-CARBOXYLATE is a quinoline derivative with the molecular formula C15H11F3N2O4. It features a hydroxy group, a trifluoromethoxy group, and an ethyl ester group, making it a versatile building block in the synthesis of pharmaceuticals and other organic compounds. Its unique structure and potential pharmacological and biological activities render it a promising candidate for drug design and development.

175203-85-7

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175203-85-7 Usage

Uses

Used in Pharmaceutical Industry:
ETHYL 4-HYDROXY-6-(TRIFLUOROMETHOXY)QUINOLINE-3-CARBOXYLATE is used as a building block for the synthesis of pharmaceuticals due to its potential pharmacological and biological activities. Its unique structure allows for the development of new medications with improved therapeutic properties.
Used in Organic Chemistry Research:
In the field of organic chemistry, ETHYL 4-HYDROXY-6-(TRIFLUOROMETHOXY)QUINOLINE-3-CARBOXYLATE is used as a key intermediate in the synthesis of complex organic molecules. Its presence in various chemical reactions contributes to the advancement of organic chemistry and the discovery of novel compounds with diverse applications.
Used in Drug Design and Development:
ETHYL 4-HYDROXY-6-(TRIFLUOROMETHOXY)QUINOLINE-3-CARBOXYLATE is employed as a component in drug design and development. Its structure and functional groups enable the creation of new molecules with potential therapeutic effects, contributing to the discovery of innovative treatments for various diseases and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 175203-85-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,5,2,0 and 3 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 175203-85:
(8*1)+(7*7)+(6*5)+(5*2)+(4*0)+(3*3)+(2*8)+(1*5)=127
127 % 10 = 7
So 175203-85-7 is a valid CAS Registry Number.
InChI:InChI=1/C13H10F3NO4/c1-2-20-12(19)9-6-17-10-4-3-7(21-13(14,15)16)5-8(10)11(9)18/h3-6H,2H2,1H3,(H,17,18)

175203-85-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 4-hydroxy-6-(trifluoromethoxy)quinoline-3-carboxylate

1.2 Other means of identification

Product number -
Other names ethyl 4-oxo-6-(trifluoromethoxy)-1H-quinoline-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:175203-85-7 SDS

175203-85-7Relevant academic research and scientific papers

4-HYDROXYQUINOLINE-3-CARBOXAMIDES AND HYDRAZIDES AS ANTIVIRAL AGENTS

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Page/Page column 35, (2010/02/13)

The present invention provides 4-hydroxyquinoline-3-carboxamide and hydrazide compounds of formula I These compounds are useful to treat or prevent the herpesviral infections, particularly, human cytomegaloviral infection.

4-hydroxyquinoline-3-carboxamides and hydrazides as antiviral agents

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, (2008/06/13)

The present invention provides 4-hydroxyquinoline-3-carboxamide and hydrazide compounds of formula I These compounds are useful to treat or prevent the herpesviral infections, particularly, human cytomegaloviral infection.

High affinity central benzodiazepine receptor ligands: Synthesis and structure-activity relationship studies of a new series of pyrazolo[4,3- c]quinolin-3-ones

Savini,Massarelli,Nencini,Pellerano,Biggio,Maciocco,Tuligi,Carrieri,Cinone,Carotti

, p. 389 - 399 (2007/10/03)

A large series of 2-aryl(heteroaryl)-2,5-dihydropyrazolo[4,3-c]quinolin- 3-(3H)-ones, carrying appropriate substituents at the quinoline and N2- phenyl rings, were prepared and tested as central benzodiazepine receptor ligands. Results from structure-affinity relationship studies were in full agreement with previously proposed pharmacophore models and, in addition, quantitative structure-activity analysis gave further significant insight into the main molecular determinants of high benzodiazepine receptor affinity. The intrinsic activity of some active ligands was also determined and preliminary discussed.

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