3913-80-2

Basic information

• Product Name: (E)-oct-2-enyl acetate
• Synonyms: (E)-oct-2-enyl acetate;TRANS-2-OCTEN-1-YLACETATE;(E)-2-Octen-1-ol acetate
• CAS NO: 3913-80-2
• Molecular Formula: C₁₀H₁₈O₂
• Molecular Weight: 170.24872
• EINECS: 223-473-7
• Mol File: 3913-80-2.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 216.8°Cat760mmHg
• Flash Point: 78.8°C
• Appearance: /
• Density: 0.892g/cm³
• CAS DataBase Reference: (E)-oct-2-enyl acetate(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-oct-2-enyl acetate(3913-80-2)
• EPA Substance Registry System: (E)-oct-2-enyl acetate(3913-80-2)

Safety Data

• Hazardous Substances Data: 3913-80-2(Hazardous Substances Data)

Usage

Description

(E)-oct-2-enyl acetate is an organic compound with a distinct green, fatty, and fruity aroma, characterized by a fresh nuance. It is commonly found in bananas and is known for its unique taste and scent properties.

Uses

Used in Flavor and Fragrance Industry:
(E)-oct-2-enyl acetate is used as a flavoring agent for its green, fatty, and fruity taste characteristics, adding a fresh nuance to various food products. Its ability to mimic the natural aroma of bananas makes it a popular choice in the creation of fruit-flavored products.
Used in Perfumery:
In the perfumery industry, (E)-oct-2-enyl acetate is utilized as a fragrance ingredient due to its fresh and fruity scent. It can be used to enhance the overall aroma of perfumes, colognes, and other scented products, contributing to a more complex and appealing fragrance profile.
Used in the Cosmetic Industry:
(E)-oct-2-enyl acetate can also be found in the cosmetic industry, where it serves as an additive to provide a pleasant and natural scent to products such as lotions, creams, and body washes. Its green, fatty, and fruity aroma can help create a more enjoyable user experience and mask any undesirable odors in these products.

Upstream product

• 42886-42-0 3-chloro-1-octene 
• 127-09-3 sodium acetate 
• 68883-76-1 (E)-1-chlorooct-2-ene 
• 2442-10-6 oct-1-en-3-yl acetate 
• 26806-12-2 (Z)-oct-2-en-1-yl acetate 
• 67007-29-8 2-(Phenylseleno)-octylacetat 
• 18409-17-1 (E)-oct-2-en-1-ol 
• 108-24-7 acetic anhydride 
• 3391-86-4 1-octen-3-ol 
• 111-66-0 oct-1-ene 
• 34837-55-3 Phenylselenyl bromide 
• 64-19-7 acetic acid 
• 75-36-5 acetyl chloride 
• 34414-28-3 (E)-1-chloro-4-acetoxybut-2-ene 

Downstream Products

• 90633-61-7 1-Methyl-4-[((E)-oct-2-ene)-1-sulfonyl]-benzene 
• 89268-74-6 1-methyl-4-(oct-1-en-3-ylsulfonyl)benzene 
• 2442-10-6 oct-1-en-3-yl acetate 
• 26806-12-2 (Z)-oct-2-en-1-yl acetate 
• 62179-16-2 (E)-1-(phenyloxy)-2-octene 
• 4124-88-3 3-nonenoic acid 
• 4436-85-5 2-vinylheptanoic acid 
• 28163-88-4 (E)-non-3-enoic acid 
• 41653-98-9 (Z)-non-3-enoic acid 
• 139775-81-8 (E)-1-(4-Methylphenyl)-2-nonen-1-one 

Relevant articles and documents

Attractant pheromone for male rice bug, Leptocorisa chinensis: Semiochemicals produced by both male and female

GC profiles of the airborne volatiles produced by adult males and females of the rice bug, L. chinensis showed no qualitative chemical dimorphism. However, GC-EAD experiments showed that eight of the compounds elicited strong responses in male and female antennae. Ruling out alarm pheromone and compounds that were not found in the whole-body extracts of the bugs, four compounds remained to be tested as possible attractants. In the field experiments, the whole mixture or tertiary blends were not attractive; however, males were strongly attracted to a 5:1 mixture of 2-(E)-octenyl acetate and octanol. The attractancy of the binary mixture was decreased by the addition of 3-(Z)-octenyl acetate. Although the binary lure specifically attracted males, there was no evidence that it triggered any response of sexual behavior in males.

Ligand-controlled regiodivergent Ni-catalyzed reductive carboxylation of allyl esters with CO2

A novel Ni-catalyzed regiodivergent reductive carboxylation of allyl esters with CO2 has been developed. This mild, user-friendly, and operationally simple method is characterized by an exquisite selectivity profile that is dictated by the ligand backbone.

Stereospecific Reduction and Cross-Coupling of γ-Monosubstituted Allylic Chlorides Using Coordinatively Unsaturated Palladium Catalysts

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