86770-78-7

Basic information

• Product Name: 2-[2-(2-{2-[2-(2-Benzyloxy-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-ethylamine
• Synonyms: 2-[2-(2-{2-[2-(2-Benzyloxy-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-ethylamine
• CAS NO: 86770-78-7
• Molecular Weight: 371.474
• Mol File: 86770-78-7.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 466.8±40.0 °C(Predicted)
• Density: 1.074±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 2-[2-(2-{2-[2-(2-Benzyloxy-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-ethylamine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[2-(2-{2-[2-(2-Benzyloxy-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-ethylamine(86770-78-7)
• EPA Substance Registry System: 2-[2-(2-{2-[2-(2-Benzyloxy-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-ethylamine(86770-78-7)

Safety Data

• Hazardous Substances Data: 86770-78-7(Hazardous Substances Data)

Usage

General Description

The chemical "2-[2-(2-{2-[2-(2-Benzyloxy-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-ethylamine" is a complex compound with a long chain of ethoxy groups connected to a central amine group. The structure of this compound consists of multiple ethoxy groups branching off from each other, leading to a highly branched and elongated molecular structure. Additionally, the presence of a benzyloxy group indicates that there is a benzene ring connected to an oxygen atom within the compound. Overall, this chemical has a long, branched structure with multiple ethoxy and benzyloxy groups, and it likely has a variety of potential uses in chemical and pharmaceutical applications.

Upstream product

• 100-39-0 benzyl bromide 
• 129086-11-9 19-Phenyl-3,6,9, 12,15,18-hexaoxanonadec-1-yl 4-methylbenzenesulfonate 
• 24342-68-5 1-phenyl-2,5,8,11,14,17-hexaoxanonadecan-19-ol 
• 2615-15-8 pentaethylene glycol 
• 86770-73-2 {2-[2-(2-{2-[2-(2-Azido-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-ethoxymethyl}-benzene 

Relevant articles and documents

Lack of effect of the length of oligoglycine- and oligo(ethylene glycol)-derived para-substituents on the affinity of benzenesulfonamides for carbonic anhydrase II in solution

Using 1H NMR spectroscopy, values of T2 have been determined for the methylene protons of the oligoglycine moieties of para-substituted benzenesulfonamides having structures H2NO2SC6H4CO(Gly)(n)OH (n = 1-6) bound at the active site of bovine carbonic anhydrase II (CA, EC 4.2.1.1). These values have been correlated with measurements of dissociation constants of these complexes, in order to infer motion of these ligands when bound to the enzyme. Motion of glycines 1-3 (those closest to the aryl ring) is hindered by their proximity to the protein; motion of glycines 4-6 is relatively unhindered. Despite the restriction to motion inferred for glycines 1-3, the values of K(d) for the six compounds (n = 1-6, 1-6) are indistinguishable within experimental uncertainty (± 20%): K(d) in μM (n) 0.30 (1); 0.26 (2); 0.33 (3); 0.37 (4); 0.37 (5); 0.34 (6). There is, therefore, an unexpected compensation of the loss in conformational entropy on binding by another contributor to the free energy.