80413-54-3

Basic information

• Product Name: 2-(acryloyloxy)ethyl 6-hydroxyhexanoate
• Synonyms: 2-(acryloyloxy)ethyl 6-hydroxyhexanoate;6-Hydroxyhexanoic acid 2-[(1-oxo-2-propenyl)oxy]ethyl ester;Einecs 279-461-7
• CAS NO: 80413-54-3
• Molecular Formula: C₉H₁₁ClO₃S
• Molecular Weight: 230.25762
• EINECS: 279-461-7
• Mol File: 80413-54-3.mol
• Article Data: 14

Chemical Properties

• Boiling Point: 343.3°C at 760 mmHg
• Flash Point: 125.7°C
• Appearance: /
• Density: 1.098g/cm³
• Vapor Pressure: 4.57E-06mmHg at 25°C
• Refractive Index: 1.463
• PKA: 15.14±0.10(Predicted)
• CAS DataBase Reference: 2-(acryloyloxy)ethyl 6-hydroxyhexanoate(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(acryloyloxy)ethyl 6-hydroxyhexanoate(80413-54-3)
• EPA Substance Registry System: 2-(acryloyloxy)ethyl 6-hydroxyhexanoate(80413-54-3)

Safety Data

• Hazardous Substances Data: 80413-54-3(Hazardous Substances Data)

Usage

Derived from

2-(acryloyloxy)ethyl acrylate and 6-hydroxyhexanoic acid

Usage

Commonly used as a monomer in the production of polymers and resins

Characteristics

Ability to form cross-linked networks

Applications

Suitable for use in adhesives, coatings, and sealants

Other uses

Used as a reactive diluent in UV-curable coatings and inks

Importance

Versatile and valuable material in the chemical industry.

InChI:InChI=1/C11H18O5/c1-2-10(13)15-8-9-16-11(14)6-4-3-5-7-12/h2,12H,1,3-9H2

Upstream product

• 98-59-9 p-toluenesulfonyl chloride 
• 107-07-3 2-chloro-ethanol 
• 13891-58-2 chloroethyl chlorosulfate 
• 108-88-3 toluene 
• 75-21-8 oxirane 
• 74-85-1 ethene 
• 7182-86-7 tetrabutylammonium p-toluenesulfonate 
• 107-04-0 1-Bromo-2-chloroethane 
• 80-48-8 methyl p-toluene sulfonate 
• 824-79-3 sodium 4-methylbenzenesulfinate 

Relevant articles and documents

Fluorescent molecule for recognizing copper ions, preparation method and application

The invention discloses a fluorescent molecule for recognizing copper ions, a preparation method and application. Polycyclic aromatic hydrocarbons such as naphthalene rings or anthracene rings are used as initial raw materials; through a series of optimized organic synthesis reaction (substitution and addition), after the connection with different recognition sites, molecular clamp body tweezer host compounds with different recognition performance can be obtained. The fluorescent molecule can be used for copper ion detection and solves the problems that the existing molecule device is difficult to effectively recognize object molecules.

BENZIMIDAZOLES AND RELATED ANALOGS AS SIRTUIN MODULATORS

Provided herein are sirtuin-modulating compounds of formula (II) The sirtuin-modulating compounds may be used for increasing the lifespan of a cell, and treating and/or preventing a wide variety of diseases and disorders including, for example, diseases or disorders related to aging or stress, diabetes, obesity, neurodegenerative diseases, cardiovascular disease, blood clotting disorders, inflammation, cancer, and/or flushing as well as diseases or disorders that would benefit from increased mitochondrial activity. Also provided are compositions comprising a sirtuin-modulating compound in combination with another therapeutic agent.

[2]Catenane Assembly from Calix[4]arene Crown Ethers

A variety of novel calix[4]arene-incorporating crown ethers with or without intramolecular hydrogen bonding have been prepared by two efficient methods and utilized as donor rings to assemble calix[4]arene [2]catenanes based on π-stacking interaction between hydroquinone and bipyridinium units. Treatment of calix[4]arene crown ethers 4, 10a, or 10b, whose cone conformation was fixed by intramolecular hydrogen bonding within the calix[4]arene moiety, with dicationic salt 15·2PF6 and dibromide 16 afforded the corresponding [2]catenanes 17a·4PF6, 17b·4PF6, and 17b·4PF6in 20%, 53%, and 55% yields, respectively, whereas from the reactions of 15·2PF6and dibromide 16 in the presence of conformationally flexible 11 or 12 with a cone conformation kept by two propyl groups, [2]catenanes 18-4PF6 and 19-4PF6 were obtained in 12% and 6% yields. [2]Catenanes 21a· 4Cl, 21b·4Cl, and 21c·4Cl, incorporating calix[4]arene in both the donor and acceptor rings, were also successfully assembled from 10a or 10b, 16, and dicationic salts 20a·2PF6 or 20b·2PF6. The dynamic 1H NMR and absorption spectra of the [2]catenanes have been investigated, which revealed a strongest donor-acceptor interaction in 17a·4PF6 and that the cone [2]catenanes 17a-c·4PF6 can isomerize to the partial cone isomer at high temperature. The difference of the dynamic properties of these catenanes was discussed. The results demonstrate that catenation is one new general method to change the conformational distributions of calix[4]arenes.