1379649-80-5

Usage

Uses

Used in Organic Synthesis:
Ethyl 3-(2-(2-hydroxyethoxy)ethoxy)propanoate is used as a reagent in organic synthesis for its ability to participate in various chemical reactions, such as esterification, transesterification, and substitution reactions. Its presence of multiple ethoxy chains and a reactive ester group make it a valuable building block for the creation of complex organic molecules and compounds.
In the Pharmaceutical Industry:
Ethyl 3-(2-(2-hydroxyethoxy)ethoxy)propanoate can be used as a reagent for the synthesis of pharmaceutical compounds, particularly those requiring the formation of ester linkages or the incorporation of ethoxy chains. Its versatility in organic synthesis allows for the development of new drug candidates with potential therapeutic applications.
In the Chemical Industry:
ethyl 3-(2-(2-hydroxyethoxy)ethoxy)propanoate can also be utilized in the chemical industry for the production of various specialty chemicals, additives, and intermediates. Its unique structure and reactivity make it suitable for the development of new materials with specific properties, such as surfactants, lubricants, or polymer additives.
In the Research and Development Sector:
Ethyl 3-(2-(2-hydroxyethoxy)ethoxy)propanoate serves as a valuable research tool for scientists and researchers working on the development of new synthetic methods, reaction mechanisms, and understanding the properties of complex organic molecules. Its unique structure and reactivity can provide insights into new areas of chemical research and innovation.

Upstream product

• 64-17-5 ethanol 
• 133803-81-3 2-methyl-2-propanyl 3-[2-(2-hydroxyethoxy)ethoxy]propanoate 

Downstream Products

• 1379649-73-6 3-(2-(2-mercaptoethoxy)ethoxy)propanoic acid 
• 1379649-81-6 ethyl 3-(2-(2-(tosyloxy)ethoxy)ethoxy)propanoate 

Relevant academic research and scientific papers

PYRROLO[2,3-B]PYRIDIN DERIVATIVES AS INHIBITORS OF INFLUENZA VIRUS REPLICATION

Provided herein are compounds of Formula A, B or C that can inhibit the replication of influenza viruses, reduce the amount of influenza viruses, and/or treat influenza.

PYRROLOPYRIMIDINE DERIVATIVES USEFUL AS INHIBITORS OF INFLUENZA VIRUS REPLICATION

Methods of inhibiting the replication of influenza viruses in a biological sample or patient, of reducing the amount of influenza viruses in a biological sample or patient, and of treating influenza in a patient, comprises administering to said biological sample or patient a safe and effective amount of a compound represented by any of Formulas l-lll, or a pharmaceutically acceptable salt thereof. A pharmaceutical composition comprises a safe and effective amount of such a compound or pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier, adjuvant or vehicle.

Rapid preparation of multifunctional surfaces for orthogonal ligation by microcontact chemistry

Microcontact chemistry has been applied to patterned glass and silicon substrates by successive reaction of unprotected and monoprotected heterobifunctional linkers with alkene-terminated self-assembled monolayers (SAMs) to produce bi-, tri-, and tetrafunctional surfaces. Photochemical microcontact printing of an azide thiol linker followed by immobilization of an acid thiol linker on an undecenyl-terminated SAM results in a well-defined, micropatterned surface with terminal azide, acid, and alkene groups. Biologically relevant molecules (biotin, carbohydrates) have been selectively attached to the surface by means of orthogonal ligation chemistry, and the resulting microarrays display selective binding to fluorescently labeled proteins. An orthogonally addressable, tetrafunctional surface (azide, acid, alkene, and amine) can be prepared by an additional printing step of a tert-butyloxycarbonyl (Boc)-protected alkyne amine linker on the azide structures by using the copper(I)-catalyzed azide-alkyne Huisgen cycloaddition and subsequent removal of the protective group. Copyright