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1,2-Bis(allyloxy) ethane, also known as allyl diglycol, is a colorless liquid chemical compound with the molecular formula C10H18O2. It has a relatively low boiling point and is commonly used as a crosslinking agent in the production of thermoset resins.

7529-27-3

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7529-27-3 Usage

Uses

Used in Adhesives Industry:
1,2-Bis(allyloxy) ethane is used as a crosslinking agent for thermoset resins, which are employed in the production of adhesives. This enhances the adhesive's bonding strength and durability.
Used in Coatings Industry:
In the coatings industry, 1,2-Bis(allyloxy) ethane serves as a crosslinking agent in thermoset resins, improving the hardness, chemical resistance, and overall performance of the coatings.
Used in Composites Industry:
1,2-Bis(allyloxy) ethane is used as a crosslinking agent in the production of composite materials, contributing to their structural integrity and mechanical properties.
Used in Epoxy Resins:
1,2-Bis(allyloxy) ethane is utilized as a reactive diluent in epoxy resins, where it can improve flexibility and impact resistance, making the final product more robust and versatile.
Used in Chemical Synthesis:
1,2-Bis(allyloxy) ethane is also used in the synthesis of other chemicals, playing a crucial role in the production of various compounds for different applications.
Used in Industrial Processes:
1,2-BIS(ALLYLOXY) ETHANE is employed in certain industrial processes, where its properties can be leveraged to achieve specific outcomes or improve process efficiency.
Safety Precautions:
Due to its potential for skin and eye irritation, as well as its flammability, proper handling and safety precautions are necessary when working with 1,2-Bis(allyloxy) ethane.

Check Digit Verification of cas no

The CAS Registry Mumber 7529-27-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,2 and 9 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7529-27:
(6*7)+(5*5)+(4*2)+(3*9)+(2*2)+(1*7)=113
113 % 10 = 3
So 7529-27-3 is a valid CAS Registry Number.

7529-27-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(2-prop-2-enoxyethoxy)prop-1-ene

1.2 Other means of identification

Product number -
Other names 4,7-dioxa-1,9-decadiene

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7529-27-3 SDS

7529-27-3Downstream Products

7529-27-3Relevant academic research and scientific papers

NOVEL TETRACARBOXYLIC DIANHYDRIDE, POLYIMIDE RESIN AND METHOD FOR PRODUCING THE SAME, PHOTOSENSITIVE RESIN COMPOSITIONS, PATTERNING PROCESS, METHOD FOR FORMING CURED FILM, INTERLAYER INSULATING FILM, SURFACE PROTECTIVE FILM, AND ELECTRONIC PARTS

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Paragraph 0279, (2019/06/17)

The present invention has been made in view of the circumstances herein. An object of the present invention is to provide: a tetracarboxylic dianhydride which can lead to a polyimide usable as a base resin of a photosensitive resin composition capable of forming a fine pattern and obtaining high resolution without impairing excellent characteristics such as mechanical strength and adhesiveness; a polyimide resin obtained by using the tetracarboxylic dianhydride; and a method for producing the polyimide resin. The tetracarboxylic dianhydride is shown by the following general formula (1).

A method of manufacturing an alkylene glycol ether (poly)

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Paragraph 0054; 0055, (2016/10/17)

PROBLEM TO BE SOLVED: To provide a method for producing a (poly)alkylene glycol diether, introducing the oxyalkylene groups of the optional mole number of addition and optional terminal alkyl groups by using a metallosilicate catalyst having 10 to 1,000 ratio of SiO2/M2O3as an ether interchange reaction catalyst. SOLUTION: This method for producing the (poly)alkylene glycol diether includes a process of obtaining the (poly)alkylene glycol diether by the ether interchange reaction of a first (poly)alkylene glycol monoether with a second (poly)alkylene glycol monoether in the presence of the metallosilicate catalyst having 10 to 1,000 ratio of SiO2/M2O3(wherein, M is ≥1 kind selected from the group consisting of Al, Ga, Ge, B, Zn, P, Zr, Ti, Cr, Be, V and As). COPYRIGHT: (C)2012,JPOandINPIT

Printable cross-linked polymer blend dielectrics. Design strategies, synthesis, microstructures, and electrical properties, with organic field-effect transistors as testbeds

Kim, Choongik,Wang, Zhiming,Choi, Hyuk-Jin,Ha, Young-Geun,Facchetti, Antonio,Marks, Tobin J.

, p. 6867 - 6878 (2008/12/23)

We report here the synthesis and dielectric properties of optimized, cross-linked polymer blend (CPB) dielectrics for application in organic field-effect transistors (OFETs). Novel silane cross-linking reagents enable the synthesis of CPB films having excellent quality and tunable thickness (from 10 to ~500 nm), fabricated both by spin-coating and gravure-printing. Silane reagents of the formula X3Si-R-SiX3 (R = -C 6H12- and X = Cl, OAc, NMe2, OMe, or R = -C2H4-O-C2H4- and X = OAc) exhibit tunable reactivity with hydroxyl-containing substrates. Dielectric films fabricated by blending X3Si-R-SiX3 with poly(4-vinyl)phenol (PVP) require very low-curing temperatures (~110°C) and adhere tenaciously to a variety of FET gate contact materials such as n +-Si, ITO, and Al. The CPB dielectrics exhibit excellent insulating properties (leakage current densities of 10-7 ~ 10-8 A cm-2 at 2.0 MV/cm) and tunable capacitance values (from 5 to ~350 nF cm-2). CPB film quality is correlated with the PVP-cross-linking reagent reactivity. OFETs are fabricated with both p- and n-type organic semiconductors using the CPB dielectrics function at low operating voltages. The morphology and microstructure of representative semiconductor films grown on the CPB dielectrics is also investigated and is correlated with OFET device performance.

Heterobifunctional multivalent inhibitor-adaptor mediates specific aggregation between Shiga toxin and a pentraxin

Solomon, Dmitry,Kitov, Pavel I.,Paszkiewicz, Eugenia,Grant, Gordon A.,Sadowska, Joanna M.,Bundle, David R.

, p. 4369 - 4372 (2007/10/03)

(Figure Presented) The first example of a multivalent heterofunctional inhibitor-adaptor, called "BAIT", is described. This multivalent inhibitor-adaptor is able to capture a "target" receptor (Shiga toxin) through its recognition of one ligand of a heterobivalent headgroup while the other ligand binds to an endogenous "trap" protein (serum amyloid P component, SAP). BAIT showed markedly enhanced inhibition of toxin activity. An efficient synthesis of this multivalent cluster containing heterobifunctional ligands was accomplished by chemical and chemoenzymatic approaches.

Crosslinking agent based on linear hydroxypolyallyl ether

-

, (2008/06/13)

An allyl type crosslinking agent for use in production of a super water-absorbent polymer comprising a polymerizable compound having a carbon-carbon double bond or a salt thereof, comprising a linear hydroxypolyallyl ether having at least one hydroxyl groups and at least two allyl groups obtained by allyletherification of hydroxyl groups in a linear polyol compound selected from the group consisting of erythritol, xylitol and sorbitol, is provided. This allyl type crosslinking agent is highly soluble in an aqueous solvent, and can give an excellent super water-absorbent polymer, which cannot be obtained in the prior arts, having high levels of both of water absorptivity under atmospheric pressure and water absorptivity under pressurized conditions are obtained.

Synthesis of oxathiacrown compounds by the reactions of sulfur dichloride with unsaturated compounds and their extraction characteristics

Abramov,Anisimov,Bobyleva

, p. 261 - 273 (2007/10/03)

Published data of the last 10-15 years on the use of the reactions of sulfur dichloride with various unsaturated compounds for the synthesis of oxathia- and thiacrown compounds and study of their extraction characteristics toward various transition and heavy metals are reviewed. Some previously unpublished results and associated experimental data are also included.

gem-Difluorocyclopropanes: An improved method for their preparation

Bessard, Yves,Mueller, Ulrich,Schlosser, Manfred

, p. 5213 - 5221 (2007/10/02)

By treatment with dibromodifluoromethane and triphenylphosphine, four unfunctionalized olefins, four enethers and one bis-enether were converted to the gem-difluorocyclopropanes 1-9. The yields were considerably increased and isomerizations at the double bonds were avoided if the reactions were carried out in the presence of a macrocyclic polyether such as "18-crown-6" and if, in addition, the reagents were employed in moderate excess.

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