34495-71-1 Usage
Description
Ethyl (Z)-oct-4-enoate is an organic compound that is known for its distinct aroma and is commonly found as a volatile flavor component in various fruits such as apple, yellow passion fruit, mango, pawpaw, and pineapple. It is characterized by its molecular structure, which includes a double bond in the (Z)-configuration, and is esterified with ethyl group.
Uses
Used in Flavor and Fragrance Industry:
Ethyl (Z)-oct-4-enoate is used as a flavoring agent for its fruity and apple-like aroma, adding a pleasant taste and scent to various food products and beverages.
Used in Aromatherapy:
Ethyl (Z)-oct-4-enoate is used as an aromatic component in aromatherapy, providing a refreshing and uplifting scent that can help create a calming and pleasant atmosphere.
Used in Cosmetics and Personal Care Products:
Ethyl (Z)-oct-4-enoate is used as a fragrance ingredient in cosmetics and personal care products, such as perfumes, lotions, and soaps, to provide a natural and appealing scent.
Used in Perfumery:
Ethyl (Z)-oct-4-enoate is used as a fixative in perfumery, helping to stabilize and prolong the scent of perfumes and colognes, giving them a longer-lasting and more complex aroma profile.
Preparation
From cis-1-pentenyl bromide via the lithium vinyl cuprates.
Check Digit Verification of cas no
The CAS Registry Mumber 34495-71-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,4,9 and 5 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 34495-71:
(7*3)+(6*4)+(5*4)+(4*9)+(3*5)+(2*7)+(1*1)=131
131 % 10 = 1
So 34495-71-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H18O2/c1-3-5-6-7-8-9-10(11)12-4-2/h6-7H,3-5,8-9H2,1-2H3
34495-71-1Relevant articles and documents
Ortho-substituted iodobenzenes as novel organocatalysts for bromination of alkenes
Braddock, D. Christopher,Cansell, Gemma,Hermitage, Stephen A.
, p. 2483 - 2485 (2008/03/28)
Suitably ortho-substituted iodobenzenes act as organocatalysts for the transfer of electrophilic bromine from N-bromosuccinimide to alkenes via the intermediacy of bromoiodinanes. The Royal Society of Chemistry 2006.