3098-92-8

Usage

Uses

Used in Fragrance and Flavor Industry:
Vinyl cinnamate is used as a key ingredient in the production of various fragrances and flavors, where it imparts a sweet, floral, and slightly spicy note. Its unique scent profile makes it a valuable addition to a wide range of products, including perfumes, colognes, and food flavorings.
Used in Pharmaceutical Industry:
Vinyl cinnamate serves as an intermediate in the synthesis of various pharmaceuticals. Its chemical properties allow it to be transformed into a range of active pharmaceutical ingredients, contributing to the development of new medications and therapies.
Used in Agrochemical Industry:
In the agrochemical sector, vinyl cinnamate is utilized as an intermediate in the production of various agrochemicals. Its versatility in chemical reactions enables the creation of compounds that can be used in pest control, crop protection, and other agricultural applications.
Used in Polymer and Resin Manufacturing:
Vinyl cinnamate is also employed in the manufacture of polymers and resins for a variety of industrial applications. Its ability to form stable polymers makes it a valuable component in the production of materials used in coatings, adhesives, and other industrial products.

InChI:InChI=1/C11H10O2/c1-2-13-11(12)9-8-10-6-4-3-5-7-10/h2-9H,1H2/b9-8+

Upstream product

• 2768-02-7 (vinyl)trimethoxylsilane 
• 621-82-9 Cinnamic acid 
• 108-05-4 vinyl acetate 

Downstream Products

• 4938-52-7 (3R)-1-hepten-3-ol 
• 1445-91-6 (S)-1-phenylethanol 
• 1454308-49-6 vinyl 3-phenyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)propanoate 
• 221688-07-9 6'-O-cinnamoyl-arbutin 
• 103-36-6 ethyl 3-phenyl-2-propenoate 
• 2021-28-5 ethyl dihydrocinnamate 
• 103-41-3 benzy cinnamate 
• 75-07-0 acetaldehyde 

Relevant academic research and scientific papers

COMPOUNDS FOR INHIBITING LIPID OXIDATION AND A METHOD FOR PRODUCING THE SAME

The present invention relates to a compound for inhibiting lipid oxidation, and a producing method thereof. The compound for inhibiting lipid oxidation is synthesized by a transesterification reaction though a vinyl reaction and a lipase-catalyzed reaction. The produced compound for inhibiting lipid oxidation has an excellent effect of inhibiting oxidation according to a total oxidation value (TOTOX) which is a combination of a P-anisidine value (P-AnV) and a peroxide value (PV) and an analysis of a thiobarbituric acid reaction substance (TBARS).COPYRIGHT KIPO 2016

Donor specificity and regioselectivity in Lipolase mediated acylations of methyl α-d-glucopyranoside by vinyl esters of phenolic acids and their analogues

Methyl α-d-glucopyranoside as a model acceptor was acylated by several phenolic and non-phenolic vinyl esters using immobilised Lipolase. Donor specificity and regioselectivity of reaction were investigated. Conversion and rate of acylation by structurally varied donors indicates that the synthetic reactivity of Lipolase corresponds to the hydrolytic activity of feruloyl esterase type A. Lipolase exhibited remarkable regioselectivity for primary position of methyl α-d-glucopyranoside. The acylation occurred exclusively at 6-O primary position when vinyl esters of phenolic acids (hydroxybenzoates, hydroxyphenylalkanoates and hydroxycinnamates) served as acyl donors (5-77%). In addition to the major 6-O-acyl products (52-79%), 2,6-di-O-acylated derivatives were isolated from reaction mixtures (2-13%) when non-phenolic donors were used (vinyl esters of fully methoxylated derivatives of phenolic acids, along with vinyl benzoates, cinnamates or some heterocyclic analogues).

Copper(II)-catalyzed esterification of arenecarboxylic acids with aryl- and vinyl-substituted trimethoxysilanes

In this paper, the copper(II)-catalyzed esterification reaction of arenecarboxylic acids with aryl- or vinyl-substituted trimethoxysilanes is described. A series of aryltrimethoxysilanes and arenecarboxylic acids worked well under this procedure, affording aryl benzoate derivatives in moderate to good yields. Notably, trimethoxy(vinyl)silanes also worked well under this procedure giving a facile and versatile method to access vinyl benzoate derivatives. Georg Thieme Verlag Stuttgart.