3098-92-8

Basic information

• Product Name: VINYL CINNAMATE
• Synonyms: VINYL CINNAMATE;CINNAMIC ACID VINYL ESTER;VINYL CINNAMATE, 95+%;VINYL CINNAMATE, 97%, STAB WITH CA 50PPM 4-METHOXYPHENOL;VINYL CINNAMATE, INHIBITOR MEHQ (50PPM);Vinyl Cinnamate (stabilized with MEHQ);3-Phenylacrylic acid vinyl ester;3-Phenylpropenoic acid ethenyl ester
• CAS NO: 3098-92-8
• Molecular Formula: C₁₁H₁₀O₂
• Molecular Weight: 174.2
• Product Categories: Alicyclic/Etch-Resistant MonomersPolymer Science;Lithography Monomers;Monomers;Self Assembly&Contact Printing;Vinyl Esters
• Mol File: 3098-92-8.mol
• Article Data: 3

Chemical Properties

• Melting Point: 125℃
• Boiling Point: 125°C 7mm
• Flash Point: 132°C
• Appearance: /
• Density: 1,071 g/cm3
• Vapor Pressure: 0.00836mmHg at 25°C
• Refractive Index: 1.5830
• Storage Temp.: 2-8°C
• Solubility: soluble in Methanol
• BRN: 2043181
• CAS DataBase Reference: VINYL CINNAMATE(CAS DataBase Reference)
• NIST Chemistry Reference: VINYL CINNAMATE(3098-92-8)
• EPA Substance Registry System: VINYL CINNAMATE(3098-92-8)

Safety Data

• Statements: 36/38
• Safety Statements: 26-36
• WGK Germany: 3
• Hazardous Substances Data: 3098-92-8(Hazardous Substances Data)

Usage

General Description

Vinyl cinnamate, also known as cinnamyl vinyl ether, is a chemical compound with the formula C11H10O2. It is a colorless to pale yellow liquid with a sweet, balsamic odor. Vinyl cinnamate is primarily used in the production of various fragrances and flavors, where it can impart a sweet, floral, and slightly spicy note. It is also used as an intermediate in the synthesis of other chemicals, such as pharmaceuticals and agrochemicals. Additionally, vinyl cinnamate is used in the manufacture of polymers and resins for various industrial applications. Overall, vinyl cinnamate has a wide range of uses in the chemical industry, particularly in the production of fragrances, flavors, and other chemical compounds.

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

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

Downstream Products

• 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 
• 1445-91-6 (S)-1-phenylethanol 
• 4938-52-7 (3R)-1-hepten-3-ol 
• 103-41-3 benzy cinnamate 
• 75-07-0 acetaldehyde 

Relevant articles and documents

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

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.