3050-69-9

Usage

Uses

Used in Food Industry:
Vinyl hexanoate is used as a flavoring agent for its fruity odor, enhancing the taste and aroma of various food products.
Used in Chemical Synthesis:
Vinyl hexanoate serves as a precursor in the synthesis of other compounds, contributing to the development of new chemical products.
Used in Polymer Production:
It is utilized in the creation of polymers, which have a wide range of applications in various industries due to their unique properties.
Used in Adhesives and Coatings Industry:
Vinyl hexanoate is used in the formulation of adhesives and coatings, providing them with specific characteristics such as adhesion, durability, and resistance to environmental factors.

InChI:InChI=1/C8H14O2/c1-3-5-6-7-8(9)10-4-2/h4H,2-3,5-7H2,1H3

Upstream product

• 75-07-0 acetaldehyde 
• 142-61-0 Hexanoyl chloride 
• 108-05-4 vinyl acetate 
• 142-62-1 hexanoic acid 
• 111-34-2 -butyl vinyl ether 
• 74-86-2 acetylene 

Downstream Products

• 78456-60-7 C₃₇H₃₂O₃ 
• 87860-35-3 (S)-2-Methyl-2-phenoxy carbinolcid 
• 64658-22-6 (R)-2-phenoxypropan-1-ol 
• 192370-02-8 (S)-(+)-phenyl-2H-azirine-2-methanol 
• 581-47-5 4-(2-pyridyl)pyridine 
• 859232-95-4 hexanoic acid 2-tert-butoxycarbonylamino-3-(tert-butyl-diphenyl-silanyloxy)-2-methyl-propyl ester 
• 138307-08-1 (+)-ethyl 3-(2-methoxyphenyl)-3-hexanoyloxypropionate 
• 333954-34-0 2-(R)-(5-chloro-2-nitrobenzyl)-3-hydroxypropyl hexanoate 
• 1083097-35-1 1-(benzylthio)ethyl caproate 
• 872298-30-1 2-(benzylthio)ethanol caproate 
• 491845-54-6 2-(4'-hydroxyphenyl)ethyl hexanoate 
• 1064639-73-1 caproic acid-3,4-dihydroxyphenylethyl ester 
• 1287247-49-7 methyl (2E,4R,5S)-4-(N-benzyl-N-methyl)amino-5-hydroxyhex-2-enoate 
• 1287247-51-1 methyl (2E,4S,5R)-4-(N-benzyl-N-methyl)amino-5-hexanoyloxyhex-2-enoate 

Relevant academic research and scientific papers

Process for Preparing Vinyl Carboxylates

The present invention relates to a process for preparing vinyl carboxylates, wherein a carboxylic acid is reacted with an alkyne compound in the presence of a catalyst which is selected from carbonyl complexes, halides and oxides of rhenium, of manganese, of tungsten, of molybdenum, of chromium and of iron and rhenium metal at a temperature of ≦300° C. The process gives the desired vinyl esters with high yield.

Synthesis of enol and vinyl esters catalyzed by an iridium complex

Enol and vinyl esters were successfully synthesized by the use of an iridium complex as a catalyst. The reaction of carboxylic acid with terminal alkynes in the presence of catalytic amounts of [Ir(cod)Cl]2 and Na2CO3 gave the corresponding 1-alkenyl esters. The addition of carboxylic acids to alkynes principally took place in the Markovnikov fashion. In addition, by the use of an Ir complex combined with NaOAc various vinyl esters were prepared through the transvinylation between carboxylic acids and vinyl acetate.