50551-10-5

Usage

Uses

Used in Organic Synthesis:
CARBAMIMIDOYL-ACETIC ACID ETHYL ESTER is used as a reagent in organic synthesis for its ability to participate in various chemical reactions, potentially aiding in the creation of new compounds or the modification of existing ones.
Used in Research and Development:
In the field of chemical research, CARBAMIMIDOYL-ACETIC ACID ETHYL ESTER is used as a subject of study to explore its properties, understand its behavior in different conditions, and identify novel applications that could benefit from its unique characteristics.
Used in Laboratory Settings:
CARBAMIMIDOYL-ACETIC ACID ETHYL ESTER is utilized in laboratories for educational purposes, allowing students and researchers to learn about its chemical properties and how it can be manipulated in controlled environments.
Used in Industrial Applications:
Depending on the outcomes of further research, CARBAMIMIDOYL-ACETIC ACID ETHYL ESTER may find use in specific industrial applications where its chemical properties offer advantages, such as in the production of pharmaceuticals, agrochemicals, or other specialty chemicals.

Upstream product

• 27317-59-5 Ethyl 3-ethoxy-3-iminopropionate 
• 64-17-5 ethanol 
• 2318-25-4 ethyl 3-ethoxy-3-iminopropanoate hydrochloride 

Downstream Products

• 1157-70-6 3-amino-5-phenoxycarbonylamino-isothiazole-4-carboxylic acid ethyl ester 
• 108290-86-4 2-amino-1H-pyrrole-3-carboxylic acid ethyl ester 
• 108290-85-3 ethyl 2-amino-5-methyl-1H-pyrrole-3-carboxylate 
• 118082-69-2 2-Amino-5-(4-chloro-phenyl)-1H-pyrrole-3-carboxylic acid ethyl ester 
• 873192-77-9 2-amino-5-(4-methylphenyl)-1H-pyrrole-3-carboxylic acid ethyl ester 
• 873192-78-0 2-[3-(2-chloro-ethyl)-ureido]-5-phenyl-1H-pyrrole-3-carboxylic acid ethyl ester 
• 873192-82-6 2-[[[(2-chloroethyl)amino]carbonyl]amino]-5-(4-methylphenyl)-1H-pyrrole-3-carboxylic acid ethyl ester 
• 873192-83-7 2-[3-(2-chloro-ethyl)-ureido]-5-(4-methoxy-phenyl)-1H-pyrrole-3-carboxylic acid ethyl ester 
• 873192-84-8 2-[3-(2-chloro-ethyl)-ureido]-5-(4-chloro-phenyl)-1H-pyrrole-3-carboxylic acid ethyl ester 
• 873192-81-5 2-[3-(2-chloro-ethyl)-ureido]-5-(2-chloro-phenyl)-1H-pyrrole-3-carboxylic acid ethyl ester 
• 873192-79-1 2-[3-(2-chloro-ethyl)-ureido]-5-o-tolyl-1H-pyrrole-3-carboxylic acid ethyl ester 
• 873192-80-4 2-[3-(2-chloro-ethyl)-ureido]-5-(2-methoxy-phenyl)-1H-pyrrole-3-carboxylic acid ethyl ester 

Relevant academic research and scientific papers

Synthesis and molecular modeling of 1H-pyrrolopyrimidine-2,4-dione derivatives as ligands for the α1-adrenoceptors

Three different series of 1H-pyrrolopyrimidine-2,4-dione derivatives were designed and synthesized as ligands for the α1-adrenergic receptors (α1-ARs). A microwave-assisted protocol was developed in order to improve purity and yields

An efficient large-scale synthesis of alkyl 5-hydroxy-pyridin- and pyrimidin-2-yl acetate

The synthesis of methyl 2-(5-hydroxy-3-methoxypyridin-2-yl)acetate and alkyl 2-(5-hydroxypyrimidin-2-yl)acetate is described. Methodology for an efficient access to 5-hydroxy-pyridin- and pyrimidin-2-yl acetate cores has been developed. Based on the difference in halogen reactivity, 5-bromo-2-chloropyridine and its pyrimidine analogue were functionalized judiciously by SNAr and palladium-catalyzed reactions. The outlined strategy provides a high-yielding route suitable for large-scale synthesis of these compounds as well as paves the way for a potential rapid access to other heterocyclic analogues.

3-Arylpiperazinylethyl-1H-pyrrolo[2,3-d]pyrimidine-2,4(3H,7H)-dione derivatives as novel, high-affinity and selective α1- adrenoceptor ligands

The discovery of a new series of selective and high-affinity α1-adrenoceptor (α1-AR) ligands, characterized by a 1H-pyrrolo[2,3-d]-pyrimidine-2,4(3H,7H)-dione system, is described in this paper. Some synthesized compounds, including 20, 22, and 30, displayed affinity in the nanomolar range for α1-ARs and substantial selectivity with respect to 5-HT1A and dopaminergic D1 and D 2 receptors. Functional assays, performed on selected derivatives, showed antagonistic properties.