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[(Vinyloxy)methyl]oxirane, also known as glycidyl vinyl ether, is a colorless liquid chemical compound with a faint ether-like odor and the molecular formula C6H8O2. It is slightly soluble in water and is recognized for its ability to undergo polymerization reactions, forming stable bonds with other compounds.

3678-15-7

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3678-15-7 Usage

Uses

Used in Polymer Production:
[(Vinyloxy)methyl]oxirane is used as a monomer for the production of various polymers and copolymers, such as polyurethanes, epoxy resins, and polyesters. Its polymerization properties make it valuable in creating materials with diverse applications.
Used in Adhesives and Coatings:
[(vinyloxy)methyl]oxirane is utilized in the formulation of adhesives and coatings due to its ability to form stable bonds with other substances, enhancing the durability and performance of these products.
Used in Industrial Applications:
[(Vinyloxy)methyl]oxirane's polymerization capabilities also make it a valuable component in various industrial applications, where its bonding properties contribute to the creation of robust and reliable materials.
However, it is important to note that [(vinyloxy)methyl]oxirane is considered a potential carcinogen and may cause irritation to the skin, eyes, and respiratory system. Therefore, proper handling and protective measures should be in place when working with this chemical to ensure safety.

Check Digit Verification of cas no

The CAS Registry Mumber 3678-15-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,7 and 8 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3678-15:
(6*3)+(5*6)+(4*7)+(3*8)+(2*1)+(1*5)=107
107 % 10 = 7
So 3678-15-7 is a valid CAS Registry Number.
InChI:InChI=1/C5H8O2/c1-2-6-3-5-4-7-5/h2,5H,1,3-4H2

3678-15-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name ((Vinyloxy)methyl)oxirane

1.2 Other means of identification

Product number -
Other names -

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:3678-15-7 SDS

3678-15-7Relevant academic research and scientific papers

Comparison of epoxy- and cyclocarbonate-functionalised vinyl ethers in radical copolymerisation with chlorotrifluoroethylene

Couture, Guillaume,Ladmiral, Vincent,Améduri, Bruno

, p. 124 - 132 (2015)

The synthesis of functional fluoropolymers is a challenging and highly sought-after objective. Fluoroolefins are indeed in their vast majority non-functional. Their specific reactivity however, can be turned into an advantage. Alternating copolymerisation

Separating material

-

, (2008/06/13)

The present invention provides a separating material producable by a) providing a solid substrate, having amino-functional groups coupled to the substrate surface, b) covalently coupling of the amino-functional groups with a thermally labile radical initiator, c) contacting the substrate surface with a solution of polymerizable monomers under conditions, where thermally initiated graft copolymerization of the monomers takes place, to form a structure of adjacent functional polymer chains on the surface of the substrate. The present invention further provides a method for the production of a separating material by a) providing a solid substrate, having amino-functional groups coupled to the substrate surface, b) covalently coupling of the amino-functional groups with a thermally labile radical initiator, c) contacting the substrate surface with a solution of polymerizable monomers under conditions, where thermally initiated graft copolymerization of the monomers takes place, to form a structure of adjacent functional polymer chains on the surface of the substrate.

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