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2-(acryloyloxy)ethyl 6-hydroxyhexanoate

  • CAS：80413-54-3
  • purity：99%
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Quality Factory Supply 99% Pure 2-(acryloyloxy)ethyl 6-hydroxyhexanoate 80413-54-3 with Efficient Delivery

  • Molecular Formula: C9H11ClO3S
  • Molecular Weight: 234.704
  • Vapor Pressure: 4.57E-06mmHg at 25°C 
  • Boiling Point: 343.3°C at 760 mmHg 
  • PKA: 15.14±0.10(Predicted) 
  • Flash Point: 125.7°C 
  • PSA： 72.83000 
  • Density: 1.098g/cm3 
  • LogP: 0.81150 

2-(acryloyloxy)ethyl 6-hydroxyhexanoate(Cas 80413-54-3) 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.

General Description

2-(acryloyloxy)ethyl 6-hydroxyhexanoate is a chemical compound with the molecular formula C13H22O4. It is derived from the reaction of 2-(acryloyloxy)ethyl acrylate and 6-hydroxyhexanoic acid. 2-(acryloyloxy)ethyl 6-hydroxyhexanoate is commonly used as a monomer in the production of polymers and resins. It is known for its ability to form cross-linked networks, making it suitable for use in adhesives, coatings, and sealants. Additionally, it is used as a reactive diluent in UV-curable coatings and inks. Its properties make it a 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

80413-54-3 Relevant articles

Fluorescent molecule for recognizing copper ions, preparation method and application

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Paragraph 0099; 0106; 0107, (2019/02/04)

The invention discloses a fluorescent mo...

Rapid transformation of sulfinate salts into sulfonates promoted by a hypervalent iodine(III) reagent

Deruer, Elsa,Hamel, Vincent,Blais, Samuel,Canesi, Sylvain

supporting information, p. 1203 - 1207 (2018/06/04)

An alternative method for forming sulfon...

BENZIMIDAZOLES AND RELATED ANALOGS AS SIRTUIN MODULATORS

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Page/Page column 87-88, (2010/04/03)

Provided herein are sirtuin-modulating c...

FUNCTIONALIZED POLYMERS USING PROTECTED THIOLS

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Page/Page column 29, (2009/05/28)

A process for the preparation of functio...

80413-54-3 Process route

sodium 4-methylbenzenesulfinate
824-79-3

sodium 4-methylbenzenesulfinate

2-chloro-ethanol
107-07-3

2-chloro-ethanol

2-chloroethyl tosylate
80-41-1

2-chloroethyl tosylate

Conditions
Conditions Yield
With [bis(acetoxy)iodo]benzene; In dichloromethane; at 20 ℃; for 0.25h;
51%
p-toluenesulfonyl chloride
98-59-9

p-toluenesulfonyl chloride

2-chloroethyl tosylate
80-41-1

2-chloroethyl tosylate

Conditions
Conditions Yield
With 2-chloro-ethanol; at 100 ℃;
95%

80413-54-3 Upstream products

  • 98-59-9
    98-59-9

    p-toluenesulfonyl chloride

  • 107-07-3
    107-07-3

    2-chloro-ethanol

  • 13891-58-2
    13891-58-2

    chloroethyl chlorosulfate

  • 108-88-3
    108-88-3

    toluene

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