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Ethyl N-[(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)acetyl]glycinate is a complex organic compound with the chemical formula C10H12N2O6. It is a derivative of pyrimidine, a heterocyclic aromatic organic compound consisting of a six-membered ring with four carbon atoms and two nitrogen atoms. The compound features a dihydropyrimidin-1(2H)-yl group, which is a reduced form of the pyrimidine ring, and an acetylated glycine moiety. This molecule is of interest in the field of medicinal chemistry, particularly in the development of potential therapeutic agents, due to its unique structure and the ability to form hydrogen bonds. Its properties and reactivity make it a candidate for further study in drug design and synthesis.

4113-90-0

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4113-90-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4113-90-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,1 and 3 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4113-90:
(6*4)+(5*1)+(4*1)+(3*3)+(2*9)+(1*0)=60
60 % 10 = 0
So 4113-90-0 is a valid CAS Registry Number.

4113-90-0SDS

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 (2-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)acetyl)glycinate

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

1.4 Supplier's details

1.5 Emergency phone number

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More Details:4113-90-0 SDS

4113-90-0Downstream Products

4113-90-0Relevant academic research and scientific papers

Reaction of 1-carboxymethyluracil with amino acid alkyl ester hydrochloride

Srivastava,Mehrotra

, p. 569 - 571 (2015/06/16)

We have synthesized derivatives of uracil 3 by the reaction of 1-carboxymethyluracil 1 and different amino acid alkyl ester hydrochloride 2 in the presence of Et3 N, DCC, HOBt. The structure of synthesized compounds was characterized by IR, 1H NMR and mass spectroscopy.

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