26553-47-9

Basic information

• Product Name: ETHYL-3-OCTENOATE
• Synonyms: ETHYL-3-OCTENOATE;ethyl (E)-oct-3-enoate;3-Octenoic acid, ethyl ester, (3E)-;Ethyl (E)-3-octenoate;(E)-3-Octenoic acid ethyl ester
• CAS NO: 26553-47-9
• Molecular Formula: C₁₀H₁₈O₂
• Molecular Weight: 170.25
• EINECS: 247-799-4
• Mol File: 26553-47-9.mol

Chemical Properties

• Boiling Point: 212.7°Cat760mmHg
• Flash Point: 75.8°C
• Appearance: /
• Density: 0.892g/cm³
• Vapor Pressure: 0.171mmHg at 25°C
• Refractive Index: 1.439
• CAS DataBase Reference: ETHYL-3-OCTENOATE(CAS DataBase Reference)
• NIST Chemistry Reference: ETHYL-3-OCTENOATE(26553-47-9)
• EPA Substance Registry System: ETHYL-3-OCTENOATE(26553-47-9)

Safety Data

• Hazardous Substances Data: 26553-47-9(Hazardous Substances Data)

Usage

Uses

Used in Food and Beverage Industry:
ETHYL-3-OCTENOATE is used as a flavor enhancer for its ability to impart a sweet and tropical aroma to products such as fruit-flavored drinks, ice cream, and candy, enhancing the overall taste and consumer experience.
Used in Perfume and Essential Oils Production:
ETHYL-3-OCTENOATE is used as a fragrance component in the production of perfumes and essential oils due to its pleasant and appealing scent, contributing to the creation of desirable and long-lasting fragrances in various personal care and household products.

InChI:InChI=1/C10H18O2/c1-3-5-6-7-8-9-10(11)12-4-2/h7-8H,3-6,9H2,1-2H3/b8-7+

Upstream product

• 623-73-4 diazoacetic acid ethyl ester 
• 693-02-7 hex-1-yne 
• 592-41-6 1-hexene 
• 5187-82-6 (ethoxycarbonylmethyl)dimethylsulfonium bromide 
• 105-36-2 ethyl bromoacetate 
• 67826-85-1 B-trans-1-hexenyl-9-borabicyclo<3.3.1>nonane 
• 1071-46-1 hydrogen ethyl malonate 
• 66-25-1 hexanal 
• 201230-82-2 carbon monoxide 
• 86537-62-4 Ethyl 1-n-butyl-2-propenyl Carbonate 
• 37746-78-4 4-bromo-trans-crotonic acid ethyl ester 
• 122-56-5 tributyl borane 
• 64-17-5 ethanol 
• 5163-67-7 (E)-oct-3-enoic acid 

Relevant articles and documents

ATTRACTION OF FEMALE MEDITERRANEAN FRUIT FLIES TO THE FIVE MAJOR COMPONENTS OF MALE-PRODUCED PHEROMONE IN A LABORATORY FLIGHT TUNNEL

Attraction and pheromonal activity of five major identified components of the male-produced sex pheromone of the Mediterranean fruit fly Ceratitis capitata to virgin laboratory-reared females was assessed in a laboratory flight tunnel. Dual-choice competi

Synthesis and properties of a stable, cationic, rhodium Lewis-acid catalyst for hydrosilation, Mukaiyama aldol and cyclopropanation reactions

The remarkably stable cationic, three-coordinate, 14-electron rhodium complex 1 has been synthesized, isolated and used as a catalyst for hydrosilation, Mukaiyama aldol and cyclopropanation reactions.

Improvement on the synthesis of (E)-alk-3-enoic acids

(E)-Alk-3-enoic acids have been prepared in high yield (85-90%) and excellent stereoselectivity (98-99%) by a modified Knoevenagel condensation of a straight carbon chain aldehyde with malonic acid, in dimethyl sulfoxide (DMSO) or dimethylformamide (DMF) at 100°C, in the presence of piperidinium acetate as catalyst. Condensation of the aldehyde with a monoester of malonic acid, under the above conditions, gave the corresponding ester of (E)-alk-3-enoic acid in high yield (76-82%) and good stereoselectivity (90-92%). Condensation of the aldehyde with cyanoacetic acid gave the β,γ-unsaturated nitrile in moderate yield (35-40%) without stereoselectivity.

Base-Induced α-Alkenylation of Ethyl Bromoacetate, Phenacyl Bromide, and Chloroacetonitrile via B-trans -1-Alkenyl-9-borabicyclononanes

B-trans-1-Alkenyl-9-borabicyclononanes, easily and quantitatively prepared by the reaction of 9-BBN with various 1-alkynes in tetrahydrofuran, undergo facile reaction with α-halo carbanions generated from ethyl bromoacetate, phenacyl bromide, and c

INFLUENCE OF HETEROAROMATIC AMINES TO KNOEVENANGEL CONDENSATION

In the Knoevenagel condensation of hexanal and malonic acid, the ratio of α,β-and β,γ-unsaturated acids was remarkably affected by the nature of tertiary amines used as a catalyst.That is, the condensation in pyridine or isoquinoline gave 2-octenoic acid selectively, whereas the condensation in 2-methylpyridine, 2,6-dimethylpyridine, or quinoline gave 3-octenoic acid as the main product.

PALLADIUM-CATALYZED DECARBOXYLATION-CARBONYLATION OF ALLYLIC CARBONATES TO GIVE β,Γ-UNSATURATED ESTERS UNDER MILD CONDITIONS

Allylic carbonates undergo facile palladium-catalyzed decarboxylation-carbonylation under mild conditions to give β,γ-unsaturated esters in high yields using palladium-phosphine complex as a catalyst.