31255-26-2

Usage

Uses

Used in Chemical Synthesis:
Ethane,1,1'-Oxybis〔2-(2-bromoethoxy)is used as an intermediate in the synthesis of various organic compounds. The bromine atoms serve as reactive sites for further chemical reactions, allowing for the creation of a wide range of molecules with different functionalities.
Used in Pharmaceutical Industry:
Ethane,1,1'-Oxybis〔2-(2-bromoethoxy)is used as a building block for the development of new pharmaceuticals. Its ability to participate in nucleophilic substitution reactions makes it a versatile component in the synthesis of complex drug molecules.
Used in Material Science:
Ethane,1,1'-Oxybis〔2-(2-bromoethoxy)can be utilized in the development of new materials with specific properties. Ethane,1,1'-Oxybis〔2-(2-bromoethoxy)-'s hydrophilic nature and reactivity can be exploited to create materials with tailored characteristics for various applications, such as in coatings, adhesives, or polymers.
Used in Drug Delivery Systems:
Similar to gallotannin, Ethane,1,1'-Oxybis〔2-(2-bromoethoxy)can be employed in drug delivery systems to improve the solubility, bioavailability, and therapeutic outcomes of certain drugs. Ethane,1,1'-Oxybis〔2-(2-bromoethoxy)-'s reactivity and hydrophilicity make it a suitable candidate for the development of novel drug carriers and delivery platforms.

Upstream product

• 123-91-1 1,4-dioxane 
• 112-60-7 Tetraethylene glycol 
• 603-35-0 triphenylphosphine 

Downstream Products

• 60147-30-0 10,13,16-tris(p-tolylsulphonyl)-1,4,7-trioxa-10,13,16-triazacyclo-octadecane 
• 60147-32-2 10,14,18-tris(p-tolylsulphonyl)-1,4,7-trioxa-10,14,18-triazacycloicosane 
• 130759-58-9 1,13-bis-1,4,7,10,13-pentaoxatridecane 
• 75953-70-7 N,N'-dibenzyl-1,11-diamino-3,6,9-trioxaundecane dihydrochloride 
• 120808-63-1 10,14,17,21-tetrakis(p-tolylsulphonyl)-1,4,7-trioxa-10,14,17,21-tetra-azacyclotricosane 
• 87338-14-5 1,13-bis(p-tolylsulfonyl)-1,13-diaza-4,7,10-trioxacyclooctadecane 
• 74461-34-0 10,16-bis(p-tolylsulphonyl)-1,4,7,13-tetraoxa-10,16-diazacyclo-octadecane 
• 120808-60-8 10,19-bis-(p-tolylsulphonyl)-1,4,7,13,16-pentaoxa-10,19-diazacyclohemicosane 
• 101210-59-7 10,22-bis(p-tolylsulphonyl)-1,4,7,13,16,19-hexaoxa-10,22-diazcyclotetracosane 
• 87338-15-6 1,13-bis(p-tolylsulfonyl)-1,13-diaza-4,7,10-trioxacyclotricosane 
• 98572-17-9 N-(p-tolylsulphonyl)-1,4,7-trioxa-10-azacyclododecane 
• 80392-32-1 [2-(2-{2-[2-(2-Methoxy-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-benzene 
• 20768-77-8 1,13-diphenyl-1,4,7,10,13-pentaoxatridecane 
• 136755-48-1 6,7,9,10,12,13,15,16-Octahydro-8,11,14-trioxa-5,17-diselena-benzocyclopentadecene 

Relevant academic research and scientific papers

Mono- and dicationic short PEG and methylene dioxyalkylglycerols for use in synthetic gene delivery systems

A range of monocationic and dicationic dioxyalkylglycerol cytofectins have been synthesised possessing methylene and short n-ethylene glycol spacers. The monocationic compounds were found to be effective in transfections when formulated as lipopolyplexes with peptide and DNA components, in particular with shorter PEG head groups which may have less effect on peptide targeting in the ternary complex. The Royal Society of Chemistry 2008.

Metal-assisted Reactions. Part 17. Ring-opening and Dimerization of Cyclic Ethers by Titanium Halides

Reaction of TiCl4 or TiBr4 with a variety of cyclic ethers gives, predominantly, products resulting from simple ring-opening or from ring-opening with simultaneous condensation to dimeric species.The variations in yields of these two kinds of products might be correlated qualitatively with an initial formation of the complex TiX4*2E (X = Cl or Br; E = cyclic ether) in which the ethers were held in a cis or trans relationship.Although such a correlation might suggest that TiCl4 but not TiBr4 exerts a template effect on the condensation, stereochemical considerations of the reaction products indicate otherwise.TiCl3 and VCl3 do not give similar results and TiF4 gives no reaction.