1907-46-6

Usage

Uses

Used in the Fragrance Industry:
3-Ethyl-5-hexen-3-ol is used as a fragrance ingredient for its fresh, green note, enhancing the scent profiles of perfumes and other scented products.
Used in the Food Industry:
3-Ethyl-5-hexen-3-ol is used as a flavoring agent to impart natural, fruity, and green flavors to various food products.
Used in the Production of Essential Oils and Aromatherapy Products:
3-Ethyl-5-hexen-3-ol is utilized in the formulation of essential oils and aromatherapy products due to its pleasant and evocative scent, contributing to the overall sensory experience and potential therapeutic benefits.
Used in the Pharmaceutical Industry:
3-Ethyl-5-hexen-3-ol has potential applications in the pharmaceutical industry, although the specific uses are not detailed in the provided materials. Its natural occurrence and unique scent profile may offer benefits in the development of pharmaceutical products.
Used in the Cosmetic Industry:
3-Ethyl-5-hexen-3-ol also has potential applications in the cosmetic industry, where its natural scent and properties could be leveraged for various cosmetic products, although the specific uses are not detailed in the provided materials.

InChI:InChI=1/C8H16O/c1-4-7-8(9,5-2)6-3/h4,9H,1,5-7H2,2-3H3

Upstream product

• 1192-17-2 2,2-diethyloxirane 
• 92-52-4 biphenyl 
• 187737-37-7 propene 
• 96-22-0 pentan-3-one 

Downstream Products

• 58888-77-0 3-ethyl-3-hydroxypentanoic acid 
• 144-62-7 oxalic acid 
• 1608-93-1 4,4-diethylbutyrolactone 
• 40844-11-9 1-((3-ethylhex-5-en-3-yloxy)methyl)benzene 
• 124-38-9 carbon dioxide 
• 64-19-7 acetic acid 
• 802294-64-0 propionic acid 
• 96-22-0 pentan-3-one 
• 1321613-68-6 C₁₅H₂₂O₂ 
• 915225-40-0 4-ethyl-4-[diphenyl(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)silyloxy]-1-hexene 

Relevant academic research and scientific papers

Carbolithiation of simple terminal and strained internal alkenes by the naphthalene and the biphenyl dianion: New modes of reactivity of highly reduced organic species in solution

Dianions derived from arenes of high reduction potential (biphenyl, naphthalene) and Li(s) can carbometallate propene, isobutene or norbornene among other alkenes, in an intermolecular fashion. This reaction runs at room temperature to afford p

Reactivity in the upper limits of the reduction potential in solution: arene dianion intermolecular carbolithiation of alkenes

Lithium salts of dianions derived from arenes of high reduction potential (biphenyl, naphthalene) can carbometallate terminal alkenes (propene, isobutene) in an intermolecular fashion, affording partially dearomatized alkylated aryl anions, which are susc

Substitution Reactions of Secondary Halides and Epoxides with Higher Order, Mixed Organocuprates, R2Cu(CN)Li2: Synthetic, Stereochemical, and Mechanistic Aspects

Higher order cuprates, represented by the general formula R2Cu(CN)Li2, are readily prepared from copper cyanide and 2 equiv of an organolithium.These novel reagents react readily and efficiently with secondary unactivated iodides and bromides affording products of substitution.Likewise, mono-, di-, and trisubstituted epoxides undergo ring opening leading to the corresponding alcohols in excellent yields.The effects of solvent, temperature, gegenion, and variations in ligands are discussed.Replacement of the second equivalent of RLi by CH3Li strongly encouragestransfer of R over CH3 in R(CH3)Cu(CN)Li2 with halides.Use of PhLi as RRLi in place of one RTLi (i.e.RT(Ph)Cu(CN)Li2) is suggested for oxirane cleavage.The stereochemical implications associated with both couplings are also addressed.