130727-46-7

Basic information

• Product Name: 3,6,9,12-Tetraoxatricos-22-en-1-ol
• CAS NO: 130727-46-7
• Molecular Formula: C19H38O5
• Molecular Weight: 346.508
• Mol File: 130727-46-7.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 3,6,9,12-Tetraoxatricos-22-en-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 3,6,9,12-Tetraoxatricos-22-en-1-ol(130727-46-7)
• EPA Substance Registry System: 3,6,9,12-Tetraoxatricos-22-en-1-ol(130727-46-7)

Safety Data

• Hazardous Substances Data: 130727-46-7(Hazardous Substances Data)

Upstream product

• 112-60-7 Tetraethylene glycol 
• 7766-50-9 1-undecen-11-ylbromide 

Downstream Products

• 850444-73-4 3,6,9,12-tetraoxatricos-22-enyl 4-tosylate 
• 5274-68-0 tetraethylene glycol n-dodecyl ether 
• 1415712-96-7 C₃₅H₅₄N₂O₉S 
• 1415713-09-5 C₂₇H₄₄O₇ 
• 1415713-08-4 C₂₈H₄₆O₇ 
• 769931-25-1 [2-(2-{2-[2-(11-tritylsulfanyl-undecyloxy)ethoxy]ethoxy}ethoxy)ethoxy]acetic acid ethyl ester 
• 769931-27-3 [2-(2-{2-[2-(11-tritylsulfanyl-undecyloxy)ethoxy]ethoxy}ethoxy)ethoxy]acetic acid 
• 130727-51-4 <1-<(methylcarbonyl)thio>undec-11-yl>tetra(ethylene glycol) 

Relevant articles and documents

Guided assemblies of ferritin nanocages: Highly ordered arrays of monodisperse nanoscopic elements

(Figure Presented) High-density arrays of highly ordered ferritin nanocages are fabricated through the guided assembly of thiol-modified ferritin on prepatterned gold nanodots, which are prepared by block copolymer micelle lithography. One and only one fe

On-demand electrochemical activation of the click reaction on self-assembled monolayers on gold presenting masked acetylene groups

We report on a new surface modification method for grafting a "dynamic" property for on-demand activation of the click reaction. Our approach utilizes the acetylene group masked with dicobalt hexacarbonyl, Co2(CO)6, which is not reactive toward the click reaction. Electrochemical treatment reveals the acetylene group on the selected region, which is then used as a chemical handle for surface functionalization via the click reaction with an azide-containing molecule. Electrochemical and chemical conversions on the surface were verified by cyclic voltammetry, X-ray photoelectron spectroscopy, and fluorescence spectroscopy. We have demonstrated immobilization of an azide-modified RGD peptide and promotion of cell adhesion/migration to the region of electrochemical induction.

Microorganism detection and analysis using carbohydrate and lectin recognition

Methods of binding and detecting a microorganism on a solid substrate. The microorganism is bound on a solid substrate covalently bound to a capture agent having a saccharide moiety. A lectin capable of binding to the microorganism and the saccharide moiety of the capture agent is added to the sample to bind the microorganism on the solid substrate. Further provided are biosensor devices, such as a quartz crystal microbalance (QCM) device or a surface plasmon resonance (SPR) device, that incorporate the solid substrate for the detection of microorganisms.

6-Aminopenicillanic acid (6-APA) derivatives equipped with anchoring arms

6-APA derivatives were considered as selective labels for the construction of bifunctional linkers dedicated to the oriented immobilization of proteins on materials. Sulbactam-like compounds (i.e., 6-β-sulfonamido-penam sulfones) and penicillin G - like compounds (i.e., para-substituted 6-β- phenylacetamido-penams) were prepared and tested as irreversible inhibitors of representative β-lactamases and D,D-peptidases, respectively. The activity of the modified antibiotics was preserved despite their substitution with various anchoring arms. The (2-nitro-4,5-dimethoxy)-benzyl esters revealed of particular interest due to their capacity to acylate BlaR-CTD without deprotection.