54149-16-5

Usage

Uses

Used in Pharmaceutical Industry:
2-(2-bromoethoxy)propane is used as a solvent and reagent for the synthesis of various pharmaceutical compounds. Its properties make it suitable for use in the development of new drugs and the improvement of existing ones, contributing to advancements in medicinal chemistry.
Used in Agricultural Products:
In the agricultural sector, 2-(2-bromoethoxy)propane serves as an intermediate in the production of agrochemicals. Its application aids in the creation of effective pesticides and other agricultural chemicals that enhance crop protection and yield.
Used as a Solvent:
2-(2-bromoethoxy)propane is utilized as a solvent in various chemical processes due to its ability to dissolve a wide range of substances. This makes it valuable in industries that require solvents for chemical reactions, extractions, and purifications.
Used as a Reagent:
As a reagent, 2-(2-bromoethoxy)propane plays a crucial role in organic synthesis, participating in reactions that lead to the formation of desired products. Its reactivity contributes to the synthesis of complex organic molecules used in various applications.

InChI:InChI=1/C5H11BrO/c1-5(2)7-4-3-6/h5H,3-4H2,1-2H3

Upstream product

• 109-59-1 2-(1-methylethoxy)-ethanol 

Downstream Products

• 926-65-8 vinyl isopropyl ether 
• 33356-22-8 Thiophosphoric acid O-ethyl ester S-(2-isopropoxy-ethyl) ester O'-p-tolyl ester 
• 33356-20-6 Thiophosphoric acid O-ethyl ester S-(2-isopropoxy-ethyl) ester O'-m-tolyl ester 
• 33356-18-2 Thiophosphoric acid O-ethyl ester S-(2-isopropoxy-ethyl) ester O'-o-tolyl ester 
• 33348-06-0 Thiophosphoric acid O-(3,5-dimethyl-phenyl) ester O'-ethyl ester S-(2-isopropoxy-ethyl) ester 
• 33356-15-9 Thiophosphoric acid O-(3,4-dimethyl-phenyl) ester O'-ethyl ester S-(2-isopropoxy-ethyl) ester 
• 33356-33-1 Thiophosphoric acid O-(2,4-dimethyl-phenyl) ester O'-ethyl ester S-(2-isopropoxy-ethyl) ester 
• 33356-25-1 Thiophosphoric acid O-ethyl ester S-(2-isopropoxy-ethyl) ester O'-(2-isopropyl-phenyl) ester 
• 33348-19-5 Thiophosphoric acid O-(4-chloro-3-methyl-phenyl) ester O'-ethyl ester S-(2-isopropoxy-ethyl) ester 
• 33356-27-3 Thiophosphoric acid O-(2-sec-butyl-phenyl) ester O'-ethyl ester S-(2-isopropoxy-ethyl) ester 
• 33348-15-1 Thiophosphoric acid O-(4-chloro-2-methyl-phenyl) ester O'-ethyl ester S-(2-isopropoxy-ethyl) ester 
• 33348-10-6 Thiophosphoric acid O-(2-chloro-4-methyl-phenyl) ester O'-ethyl ester S-(2-isopropoxy-ethyl) ester 
• 33348-23-1 Thiophosphoric acid O-(4-chloro-3,5-dimethyl-phenyl) ester O'-ethyl ester S-(2-isopropoxy-ethyl) ester 
• 33348-30-0 Thiophosphoric acid O-(4-tert-butyl-2-chloro-phenyl) ester O'-ethyl ester S-(2-isopropoxy-ethyl) ester 

Relevant academic research and scientific papers

Catalytic Activity of Thiolate-Bridged Diruthenium Complexes Bearing Pendent Ether Moieties in the Oxidation of Molecular Dihydrogen

Thiolate-bridged diruthenium complexes bearing pendent ethers have been found to work as effective catalysts toward the oxidation of molecular dihydrogen into protons and electrons in water. The pendent ether moiety in the complex plays an important role to facilitate the proton transfer between the metal center and the external proton acceptor.

Pyranouidole Derivatives and the Use Thereof for the Treatment of Hepatitis C Virus Infection or Disease

The invention is directed to novel pyranoindole derivatives and analogs as well as compositions containing the same and to the use thereof for the treatment, prevention or inhibition of viral infections and associated diseases caused by the Hepatitis C vi