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Product Information

Product Name
Ethyl trans-2-octenoate
Brand Name
Chem Impex
Product Number
39060
CAS
7367-82-0
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
5364399
IUPAC Name
ethyl (E)-oct-2-enoate
InChI Key
AISZSTYLOVXFII-CMDGGOBGSA-N
SMILES
CCCCC/C=C/C(=O)OCC

Application

Ethyl trans-2-octenoate is widely utilized in research focused on:

Flavor and Fragrance Industry: This compound is commonly used as a flavoring agent in food products and as a fragrance in cosmetics, providing a fruity and floral aroma that enhances sensory experiences.

Perfume Formulation: Its unique scent profile makes it a popular choice in the formulation of perfumes, allowing for the creation of complex fragrance blends that appeal to consumers.

Research in Organic Chemistry: Ethyl trans-2-octenoate serves as a valuable intermediate in organic synthesis, facilitating the production of other chemical compounds and enabling researchers to explore new chemical reactions.

Biotechnology Applications: In biotechnological research, this compound can be used as a substrate for microbial fermentation, aiding in the development of bio-based products and sustainable processes.

Cosmetic Products: Its properties make it suitable for use in skincare formulations, where it can enhance texture and provide a pleasant scent, improving overall product appeal.

References Data Source From Pubchem

Hydrogenation of Internal Alkynes to E-Alkenes via Heterogeneous Catalysis

Publication Name: Science of Synthesis
Publication Date: 2023

Characterization of the key aroma compounds of a sweet rice alcoholic beverage fermented with Saccharomycopsis fibuligera

Publication Name: Journal of Food Science and Technology
Publication Date: 2020-10-08
DOI: 10.1007/s13197-020-04833-4

Medium chain unsaturated fatty acid ethyl esters inhibit persister formation of Escherichia coli via antitoxin HipB

Publication Name: Applied Microbiology and Biotechnology
Publication Date: 2018-08-07
DOI: 10.1007/s00253-018-9271-3

Dihydroxylation of Olefins with Potassium Permanganate Catalyzed­ by Imidazolium Salt

Publication Name: Synthesis
Publication Date: 2018-02-12
DOI: 10.1055/s-0036-1591763

Diisobutylaluminum Hydride Reduction

Publication Name: Science of Synthesis
Publication Date: 2018