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127286-04-8

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127286-04-8 Usage

General Description

4-Oxo-1,4-dihydro-quinoline-6-carboxylic acid ethyl ester, also known as ethyl 4-oxo-1,4-dihydroquinoline-6-carboxylate, is a chemical compound with the molecular formula C13H13NO3. It is a derivative of quinoline and is commonly used in organic synthesis and medicinal chemistry. 4-Oxo-1,4-dihydro-quinoline-6-carboxylic acid ethyl ester is known for its potential pharmacological activities, including antitumor and antibacterial properties. It is often utilized in the development of pharmaceutical drugs and research studies due to its versatile chemical structure and biological activities. Additionally, this compound has also been studied for its potential applications in materials science and related fields.

Check Digit Verification of cas no

The CAS Registry Mumber 127286-04-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,2,8 and 6 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 127286-04:
(8*1)+(7*2)+(6*7)+(5*2)+(4*8)+(3*6)+(2*0)+(1*4)=128
128 % 10 = 8
So 127286-04-8 is a valid CAS Registry Number.

127286-04-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-ethoxycarbonyl-4(1H)-quinolone

1.2 Other means of identification

Product number -
Other names Ethyl 4-oxo-1,4-dihydroquinoline-6-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:127286-04-8 SDS

127286-04-8Relevant articles and documents

Enantioselective Total Synthesis of (-)-Martinellic Acid

Pappoppula, Mukesh,Aponick, Aaron

, p. 15827 - 15830 (2015)

An enantioselective total synthesis of martinellic acid is described. The pyrroloquinoline alkaloid core is efficiently prepared from a quinoline, employing a method which relies on a newly developed Cu-catalyzed enantioselective alkynylation using the ch

Compounds and Methods of Treatment

-

Page/Page column 25, (2008/12/08)

A derivative, which is useful as a ret kinase inhibitor is described herein. The described invention also includes methods of using the same in the treatment of diseases mediated by inappropriate ret kinase activity.

4(1H)-quinolone derivatives

-

, (2008/06/13)

Quinolone derivatives having a quinolone structure: STR1 where Yo is O or S are disclosed, which are useful as cardiotonic agents. Typical examples of the quinolone derivatives include: 6,7-dimethoxy-4 (1H) quinolone (compound 6) and 5-hydroxy-6-methoxy-4(1H) quinolone (compound 1) as typical compounds of the formulae[I] and [I'], respectively, shown in the specification.

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