86259-56-5

Usage

Molecular structure

A long hydrocarbon chain with five oxygen atoms interspersed along its length, and a six-carbon aromatic ring (phenyl group).

Derivative of fatty acid

It is a modified version of a fatty acid, which is a major component of lipids and has essential biological functions.

Aromatic and hydrophobic properties

The presence of the phenyl group gives the compound the ability to interact with other molecules in biological systems.

Polar and potentially reactive

The presence of five oxygen atoms makes the compound more polar and potentially more reactive in biological processes.

Complex molecule

It is a complex molecule with potential implications for biological and chemical research.

Upstream product

• 112-60-7 Tetraethylene glycol 
• 100-44-7 benzyl chloride 
• 86259-87-2 1-phenyl-2,5,8,11-tetraoxatridecan-13-ol 
• 344567-43-7 (2-{2-[2-(2-Benzyloxy-ethoxy)-ethoxy]-ethoxy}-ethoxy)-acetic acid ethyl ester 

Relevant academic research and scientific papers

LIVER X RECEPTOR AGONISTS AND USES THEREOF

Disclosed herein are antibody drug conjugates having an antibody or antibody fragment that binds a cell surface molecule on a target cell, wherein the target cell is a lymphocyte and a therapeutic agent that has a therapeutic effect in a subject in need t

Azethoxyl Nitroxide Spin-Labeled Crown Ethers and Cryptands with the N-O. Group Positioned near the Cavity

We report the synthesis and complexation properties of several nitroxide spin-labeled crown ethers and cryptands in which the N-O. group, in certain conformations, is thrust toward the cavity of the molecule.While initial approaches involving the cyclization of various unsymmetrically substituted tetraethylene glycols (e.g, 10, 11, and 15) were not promising, success was achieved by the sequential addition of substituted phenyl groups to nitrone 28, leading to nitroxide crown ethers 37 and 38.Nitroxide cryptand 60 was prepared by diacylation of diaza-18-crown-6 51 with azethoxyl nitroxide diacid chloride 57 followed by reduction.The ESR spectrum aN values of these nitroxides were not sensitive to the presence of K+, Na+, or Li+ in MeOH, While diaza-18-crown-6, decamethylene cryptand 55, and nitroxide cryptand 60 formed 1:1 complexes with NaBPh4 in CDCl3, nitroxide crown ethers 37 and 38 and amide 54 did not.Adaption of the quantitative methodology of Cram et al. showed that 55 and 60 bind Na+ somewhat better than dicyclohexyl-18-crown-6.K+ is bound better than Na+ by 55 and 60, tough not as strongly as dicyclohexyl-18-crown-6.The binding of K+ and Na+ by 37 and 38 is minimal.