105891-55-2

Usage

Long-chain polyether

It is a compound with a long, linear structure consisting of multiple ether groups (-O-).

Diphenyl compound

It contains two benzene rings, which are connected to the main chain.

10 oxygen atoms

The compound has a total of 10 oxygen atoms, which are part of the ether groups.

36 carbon atoms

The compound's structure consists of 36 carbon atoms, forming the backbone of the molecule.

Building block in organic synthesis

It is primarily used as an intermediate compound to create more complex molecules in organic chemistry.

Potential applications

The compound may have uses in various industries, such as pharmaceuticals, materials science, and agricultural chemistry.

Versatile compound

Due to its unique structure and properties, 2,5,8,11,14,17,20,23,26,29-Decaoxatriacontane, 1,30-diphenylcan be adapted for multiple purposes and applications.

Upstream product

• 60389-48-2 C₂₄H₃₄O₆ 
• 100-44-7 benzyl chloride 
• 86259-87-2 1-phenyl-2,5,8,11-tetraoxatridecan-13-ol 
• 4792-15-8 Pentaethylene glycol 
• 112-60-7 Tetraethylene glycol 
• 55489-58-2 triethylene glycol monobenzyl ether 
• 84131-04-4 triethylene glycol monobenzyl tosyl ether 
• 112-27-6 2,2'-[1,2-ethanediylbis(oxy)]bisethanol 
• 80322-82-3 triethyleneglycol dimesylate 
• 57671-28-0 2-(2-{2-[2-(2-benzyloxyethoxy)ethoxy]ethoxy}ethoxy)ethanol 
• 105891-51-8 (2-{2-[2-(2-Chloro-ethoxy)-ethoxy]-ethoxy}-ethoxymethyl)-benzene 

Downstream Products

• 361543-07-9 1,2-bis-(2-{2-[2-(2-azido-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethane 
• 3386-18-3 nonaethylene glycol 

Relevant academic research and scientific papers

Synthesis of oligo(ethylene glycol) toward 44-mer

A synthetic method for oligo(ethylene glycol) toward 44-mer (FW = 1956.35) is described. Reiteration of Williamson's ether synthesis and hydrogenation to remove protecting benzyl group affords desired oligo(ethylene glycol) toward 44-mer in moderate yields. The advantages in this method are use of commercially easily available materials as starting materials and procedures avoiding difficulty in purification of the products as much as possible.

Synthesis and analysis of polyethylene glycol linked P-glycoprotein-specific homodimers based on (-)-stipiamide

A series of five homodimeric polyethylene glycol (PEG) linked homodimers based on the multidrug resistance reversal agent (-)-stipiamide were made and tested for their ability to interact with P-glycoprotein, the protein responsible for multidrug resistance, using ATPase and photoaffinity displacement assays. Key reactions include a new alkoxide-mesylate displacement for the assembly of the PEG linkers and a double Sonogashira coupling reaction.

A NOVEL, UNEQUIVOCAL SYNTHESIS OF POLYETHYLENE GLYCOLS

Unequivocal synthesis of polyethyleneglycols is presented.The key step for this synthesis is the selective monobenzylation of oligoethyleneglycols by the phase transfer catalysis technique.