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2-OXO-3-QUINOLIN-2-YL-PROPIONIC ACID ETHYL ESTER is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13119-76-1

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13119-76-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13119-76-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,1 and 9 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 13119-76:
(7*1)+(6*3)+(5*1)+(4*1)+(3*9)+(2*7)+(1*6)=81
81 % 10 = 1
So 13119-76-1 is a valid CAS Registry Number.
InChI:InChI=1/C14H13NO3/c1-2-18-14(17)13(16)9-11-8-7-10-5-3-4-6-12(10)15-11/h3-8H,2,9H2,1H3

13119-76-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-oxo-3-quinolin-2-ylpropanoate

1.2 Other means of identification

Product number -
Other names [2]quinolyl-pyruvic acid ethyl ester

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:13119-76-1 SDS

13119-76-1Relevant academic research and scientific papers

Tricyclic derivative inhibitor as well as preparation method and applications thereof

-

Paragraph 0354; 0357-0360, (2019/06/13)

The invention relates to a tricyclic derivative inhibitor as well as a preparation method and applications thereof, in particular to a compound shown in a general formula (I) in the description, a preparation method of the compound, pharmaceutical composi

A convenient synthesis of alkyl heteroarylpyruvates

Zupet,Tisler

, p. 2245 - 2251 (2007/10/02)

Several ethyl heteroarylpyruvates were obtained by condensation of the corresponding methyl substituted azines or azoles with diethyl oxalate and in the presence of potassium tert-butoxide. The obtained compounds exist exclusively or predominantly in the enol form.

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