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(3E)-3-{hydroxy[(2-methylphenyl)amino]methylidene}quinoline-2,4(1H,3H)-dione is a complex organic compound with a molecular formula of C20H15N2O3. It features a quinoline core, which is a tricyclic aromatic system, with a hydroxy group, a 2-methylphenyl group, and an amino group attached to it. The compound is characterized by a double bond (E configuration) between the quinoline and the hydroxy[(2-methylphenyl)amino]methylidene moiety. This molecule is known for its potential applications in medicinal chemistry, particularly as a precursor or intermediate in the synthesis of various pharmaceuticals. Its structure and properties make it a subject of interest for researchers exploring new drug candidates and chemical entities.

5236-60-2

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5236-60-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5236-60-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,3 and 6 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5236-60:
(6*5)+(5*2)+(4*3)+(3*6)+(2*6)+(1*0)=82
82 % 10 = 2
So 5236-60-2 is a valid CAS Registry Number.

5236-60-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1(2H)-Pyrimidineacetic acid, 3,4-dihydro-2,4-dioxo-, methyl ester

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

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More Details:5236-60-2 SDS

5236-60-2Relevant academic research and scientific papers

Synthesis of 4-thiouracil KPGEPGPK analogues as potential TIIICBP identification tools

Pires, Viviane Silva,Da Nascimento, Sophie,Sonnet, Pascal

experimental part, p. 257 - 266 (2011/10/09)

In this paper, we described the synthesis of three octapeptides analogues which are obtained by the incorporation of photochemical 4-thiouracil (s 4U) probes selectively activables. This probe has been incorporated at the 1 and/or 3 positions in KPGEPGPK sequence since it has been demonstrated that those positions could be mutated without major anti-thrombotic activity modifications. These analogues could be used to identify a new receptor for type III collagen named Type III Collagen Binding Protein (TIIICBP).

A convenient, high-yield synthesis of 1-substituted uracil and thymine derivatives

Rejman, Dominik,Kova?ková, Soňa,Pohl, Radek,Dra?ínsky, Martin,Fiedler, Pavel,Rosenberg, Ivan

experimental part, p. 8513 - 8523 (2010/01/06)

Novel reagents for the synthesis of 1-substituted uracil and thymine derivatives have been developed. The aminolysis of 2- or 4-nitrophenyl 3-ethoxyacryloylcarbamate and 3-ethoxy-2-methylacryloylcarbamate with a variety of primary amino derivatives procee

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