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Ethyl 3-methyl-2-phenyl-quinoline-4-carboxylate is a complex organic chemical compound with the molecular formula C20H17NO2. It is a derivative of quinoline, a heterocyclic compound with a tricyclic structure consisting of a benzene ring fused to a pyridine ring. The molecule features a methyl group at the 3-position, a phenyl group at the 2-position, and a carboxylate group at the 4-position, attached to an ethyl ester. ethyl 3-methyl-2-phenyl-quinoline-4-carboxylate is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as its use as an intermediate in the production of certain dyes and pigments. Its chemical properties and reactivity make it a valuable component in the development of new compounds with specific therapeutic or industrial applications.

5471-16-9

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5471-16-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5471-16-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,7 and 1 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5471-16:
(6*5)+(5*4)+(4*7)+(3*1)+(2*1)+(1*6)=89
89 % 10 = 9
So 5471-16-9 is a valid CAS Registry Number.
InChI:InChI=1/C19H17NO2/c1-3-22-19(21)17-13(2)18(14-9-5-4-6-10-14)20-16-12-8-7-11-15(16)17/h4-12H,3H2,1-2H3

5471-16-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 3-methyl-2-phenylquinoline-4-carboxylate

1.2 Other means of identification

Product number -
Other names 3-Methyl-2-phenyl-chinolin-4-carbonsaeure-aethylester

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

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More Details:5471-16-9 SDS

5471-16-9Relevant academic research and scientific papers

Synthesis and Antimicrobial Activity of 1,3,4-Oxadiazole-2(3H)-thione and Azidomethanone Derivatives Based on Quinoline-4-carbohydrazide Derivatives

Mohamed, Mansoura I.,Kandile, Nadia G.,Zaky, Howida T.

, p. 35 - 43 (2017/02/03)

A new series compounds of quinoline derivatives were synthesized by reaction of 3-(carboxymethyl)-2-arylquinoline-4-carboxylic acids 1a, 1b, 1c with different nucleophiles. The structures of the new compounds were elucidated on the basis of FTIR,1/s

Synthesis of brequinar analogue inhibitors of malaria parasite dihydroorotate dehydrogenase

Boa, Andrew N.,Canavan, Shane P.,Hirst, Paul R.,Ramsey, Christopher,Stead, Andrew M.W.,McConkey, Glenn A.

, p. 1945 - 1967 (2007/10/03)

A series of 2-phenyl quinoline-4-carboxylic acid derivatives related to brequinar, an inhibitor of human dihydroorotate dehydrogenase (DHODH), has been prepared and evaluated as inhibitors of DHODH from the malaria parasite Plasmodium falciparum. Brequinar was essentially inactive against PfDHODH (IC50 880 μM) whereas several members of the series inhibited PfDHODH. Unexpectedly, replacement of the carboxylic acid required for brequinar to inhibit hDHODH was not essential in the diisopropylamides that inhibited PfDHODH.

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