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Usage

Uses

Used in Perfumery Industry:
6,10-dimethyl-3-propan-2-ylidene-spiro[4.5]dec-9-en-8-one is used as a key ingredient in the perfume industry for its unique woody, earthy scent. It is a component of Vetiver essential oil, which is highly esteemed as a basic ingredient in modern perfumery. 6,10-dimethyl-3-propan-2-ylidene-spiro[4.5]dec-9-en-8-one's distinct aroma profile contributes to the creation of various fragrances, enhancing their complexity and appeal.
Used in Flavor Industry:
6,10-dimethyl-3-propan-2-ylidene-spiro[4.5]dec-9-en-8-one is also used in the flavor industry to impart a woody, earthy taste to various food and beverage products. Its unique flavor profile can be used to create a wide range of flavors, from natural to synthetic, adding depth and complexity to the final product.
Used in Aromatherapy:
In aromatherapy, 6,10-dimethyl-3-propan-2-ylidene-spiro[4.5]dec-9-en-8-one is used for its potential therapeutic benefits. Its woody, earthy scent is believed to have calming and grounding effects, helping to reduce stress and anxiety. It can be used in various forms, such as essential oils, candles, and diffusers, to create a soothing and relaxing atmosphere.
Used in Cosmetics Industry:
6,10-dimethyl-3-propan-2-ylidene-spiro[4.5]dec-9-en-8-one is used in the cosmetics industry for its unique scent and potential skin care benefits. It can be incorporated into various cosmetic products, such as perfumes, body lotions, and creams, to provide a distinct and appealing fragrance while also offering potential skin care benefits.
Used in Research and Development:
6,10-dimethyl-3-propan-2-ylidene-spiro[4.5]dec-9-en-8-one is also of interest to researchers and scientists in the field of organic chemistry. Its unique molecular structure and chemical properties make it a valuable compound for studying various chemical reactions and processes, as well as for developing new applications and products in various industries.

InChI:InChI=1/C15H22O/c1-10(2)13-5-6-15(9-13)11(3)7-14(16)8-12(15)4/h7,12H,5-6,8-9H2,1-4H3/t12-,15+/m1/s1

Upstream product

• 117711-45-2 (5R,10R)-(-)-3-methyl-3-<1-acetyl-3-(1-methylethylidene)cyclopentyl>propyl mesitoate 
• 117711-46-3 (5R,10R)-(-)-3-methyl-3-<1-(1-methylethenyl)-3-(1-methylethylidene)cyclopentyl>propyl mesitoate 
• 117711-44-1 (S)-(+)-p-anisylpentenolide sulfoxide 
• 117711-43-0 (5R,10R)-(-)-10-methyl-2-(1-methylethenyl)-7-oxaspiro<4.5>decan-6-one 
• 117711-47-4 (5R,10R)-(-)-γ-methyl-3-(1-methylethenyl)-1-(1-methylethylidene)cyclopentanepropanol 
• 117711-42-9 (R)-3-((R)-1-Isopropenyl-3-isopropylidene-cyclopentyl)-butyraldehyde 
• 42091-47-4 2-Isopropylidenebutane-1,4-diol 
• 61898-55-3 (4R)-4-methyltetrahydro-2H-pyran-2-one 
• 85221-99-4 2-methyl-3-(bromomethyl)-5-bromo-2-pentene 
• 22196-46-9 (±)-β-vetivone 
• 220094-82-6 C₂₃H₃₃NO₂S 
• 50628-17-6 (5R,10R)-(-)-10-methyl-6-methylene-2-(1-methylethenyl)spiro<4.5>decan-8-ol 
• 917-54-4 methyllithium 
• 121960-43-8 (5R,10R)-2-Isopropylidene-10-methyl-spiro[4.5]dec-7-en-6-one 

Downstream Products

• 34557-54-5 methane 
• 529-08-8 vetivazulene 
• 50-00-0 formaldehyd 
• 64-18-6 formic acid 
• 15719-64-9 methylammonium carbonate 
• 67-64-1 acetone 

Relevant academic research and scientific papers

Structure/odor relationships of (-)- and (+)-β-vetivone, and their demethyl derivatives: Short communication

(-)-β-Vetivone ((-)-3a), one of the main constituents of vetiver oil, was submitted to a structure/odor relationship study. The influence of the Me groups at the cyclohexenone ring and of the configuration on the odor was examined. Detailed 1H- and 13C-NMR-spectroscopic data were collected, and the absolute configurations were determined by CD methods.

An Asymmetric Total Synthesis of Fragrant Spirodecane Sesquiterpene (-)-β-Vetivone via an Enantiomerically Pure Vinylic Sulfoxide

A nonenzymatic asymmetric synthesis of (R)-(+)-3-methylpentanolide 4 in 93percent enantiomeric purity has been achieved involving novel methyltitanium triisopropoxide conjugate methyl addition to enantiomerically pure p-anisylpentenolide sulfoxide (S)-(+)-5b.One step, five-membered ring spiroannulation then formed a quaternary carbon center in a stereospecific fashion to give spiroheterocycle (-)-3.Spiroheterocycle (-)-3 was converted directly into natural spirocarbocycle (-)-β-vetivone, 1, constituting the third asymmetric total synthesis of this commercially valuable fragrant sesquiterpene.

A Facile Synthesis of (-)-β-Vetivone

A short step synthesis of the title compound from (R)-(-)-5-trimethylsilyl-2-cyclohexenone via stereoselective intramolecular alkylation is described.