10500-08-0

Usage

Uses

Used in Coatings Industry:
1-Ethylvinyl acetate is used as a reactive diluent in the formulation of coatings to enhance their performance and durability. It aids in the crosslinking process, which strengthens the coating and improves its resistance to wear and environmental factors.
Used in Adhesives Industry:
In the adhesives industry, 1-ethylvinyl acetate is utilized as a reactive diluent and crosslinking agent. It helps in formulating adhesives with improved bonding strength and resistance to various environmental conditions, ensuring a longer-lasting and more reliable adhesive.
Used in Sealants Industry:
1-Ethylvinyl acetate is employed as a reactive diluent in the production of sealants. Its crosslinking properties contribute to the development of sealants with enhanced elasticity, adhesion, and resistance to weathering, making them suitable for various sealing applications.
Used in Textile Industry:
1-Ethylvinyl acetate is used in the production of vinyl acetate-ethylene copolymers, which find applications in the textile industry. These copolymers are utilized in the manufacturing of various textile products, such as nonwovens, providing improved strength and durability.
Used in Polymer Production:
1-Ethylvinyl acetate is also used in the production of vinyl acetate-ethylene copolymers, which have a wide range of applications, including coatings, adhesives, and textiles. These copolymers offer unique properties, such as flexibility, adhesion, and compatibility with various substrates, making them valuable in numerous industries.
Safety Precautions:
It is crucial to handle 1-ethylvinyl acetate with care, as it can be harmful if inhaled or swallowed and can cause irritation to the skin and eyes. Proper safety measures, such as wearing protective gear and ensuring proper ventilation, should be taken during its use and storage.

InChI:InChI=1/C6H10O2/c1-4-5(2)8-6(3)7/h2,4H2,1,3H3

Upstream product

• 463-51-4 Ketene 
• 78-93-3 butanone 
• 108-22-5 Isopropenyl acetate 
• 107-00-6 but-1-yne 
• 64-19-7 acetic acid 
• 1600-27-7 mercury(II) diacetate 

Downstream Products

• 1007-32-5 benzyl ethyl ketone 

Relevant academic research and scientific papers

Highly enantioselective Rh-catalysed hydrogenation of 1-alkyl vinyl esters using phosphine-phosphoramidite ligands

MatPhos, a good mate for hard tasks: The asymmetric hydrogenation of 1-alkyl vinyl esters, thwarted so far by mediocre ee values and low activities, can now be achieved with MatPhos/Rh catalysts with ee values of 96-99 % for a variety of substrates at low catalyst loadings (0.1-1 mol %) and under mild conditions (5-20 bar H2, room temperature). After hydrolysis, the corresponding chiral secondary alkyl alcohols can be obtained in high enantiopurities providing a general and practical route to this important product class. Copyright

Indole-2-carboxamide derivatives useful as beta-2 agonists

The invention relates to indole derivatives of general formula: and to processes for the preparation of, intermediates used in the preparation of, compositions containing and the uses of, such derivatives. The indole derivatives according to the present invention are useful in numerous diseases, disorders and conditions. In particular inflammatory, allergic and respiratory diseases, disorders and conditions.

Arylation and 1-Alkenylation on α-Position of Ketones via Tributyltin Enolates Catalyzed by Palladium Complex

The reaction of tributyltin enolates, prepared from tributyltin methoxide and enol acetates in situ, with aryl and 1-alkenyl bromides in the presence of dichlorobis(tri-o-tolylphosphine)palladium was found to give α-aryl and α-(1-alkenyl) ketones, respectively, in good yields with essentially complete retention of the enol acetate regiochemistry.

Process for the preparation of unsaturated ketones

Ketones, which are intermediates in the synthesis of vitamin A or perfumes, and have the general formula: EQU1 wherein R1 is hydrogen or C1-10 hydrocarbon, R2 and R3 are hydrogen or C1-4 alkyl, R4 and R5 are hydrogen or together form a --CH2 --CH2 --C(CH3)2 -- group, R6 and R7 are hydrogen or C1-10 hydrocarbon, or together with the carbon atom to which they are joined form a hydrocarbon ring of up to 10 carbons, or EQU2 forms a hydrocarbon ring of up to 10 carbons joined through R6 and R8 or R7 and R8, R8 is hydrogen or C1-10 hydrocarbon and n is 0-6, are prepared by reacting an unsaturated halide of formula EQU3 wherein X is halogen, with an enol ester of formula EQU4 wherein R9 is C1-20 hydrocarbon, in the presence of a metal catalyst.