54868-48-3

Usage

Uses

Used in the Fragrance Industry:
(E)-5-isopropyl-8-methylnona-6,8-dien-2-one is used as a key ingredient in the formulation of perfumes and fragrances for its sweet, floral scent. Its natural origin and appealing odor make it a desirable component in creating a wide range of fragrances.
Used in the Pharmaceutical Industry:
In the pharmaceutical sector, (E)-5-isopropyl-8-methylnona-6,8-dien-2-one is used as an active compound or a component in the development of various medications. Its specific application may vary depending on the therapeutic area, but its potential in this industry highlights its versatility and value.
Used in the Flavoring Industry:
(E)-5-isopropyl-8-methylnona-6,8-dien-2-one is also utilized in the flavoring industry to enhance the taste and aroma of different products. Its sweet, floral note can be an asset in creating unique and appealing flavors for the food and beverage sector.

InChI:InChI=1S/C13H22O/c1-10(2)6-8-13(11(3)4)9-7-12(5)14/h6,8,11,13H,1,7,9H2,2-5H3/b8-6+

Upstream product

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• 67-68-5 dimethyl sulfoxide 
• 57934-86-8 (+/-)-8-hydroxy-5-isopropyl-8-methyl-6(E)-nonen-2-one 
• 70687-50-2 4-isopropylglutaraldehydonitrile 
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• 4462-09-3 N-isopentylpiperidine 
• 27758-66-3 2-Isopropyl-4-ethoxycarbonylbutyraldehyd 
• 676-58-4 methylmagnesium chloride 
• 590-86-3 isovaleraldehyde 
• 51840-50-7 1-(3-methylbut-1-en-1-yl)piperidine 
• 51533-70-1 diethyl (2-methylallyl)phosphonate 
• 15303-46-5 (rac)-2-isopropyl-5-oxohexanal 

Relevant academic research and scientific papers

Facile preparation of conjugated dienes from allylic alcohols

An efficient two-step procedure to prepare conjugated dienes from allylic alcohols is developed without the formation of regioisomers and rearranged products.

Stereoselective and Modular Assembly Method for Heterocycle-Fused Daucane Sesquiterpenoids

A stereoselective synthetic method is reported for the molecular framework found in common daucane and isodaucane sesquiterpenoid natural products. The synthetic method constitutes a scalable, modular, and also asymmetric access to a complex natural product scaffold, wherein the substitution pattern and the stereochemistry can be adjusted simply by choosing different starting materials. The method allows the rapid introduction of diverse heterocyclic substructures such as (benzo)furans, (benzo)thiophenes, dithiins, thiazoles, and indoles, which actually also facilitate and direct the key intramolecular annulation step.

Preparation method of solanone and synthetic intermediate thereof

The invention relates to a preparation method of solanone and a synthetic intermediate thereof and provides a safe industrial method using not many steps to prepare a large amount of solanone as a flavor compound. The solution comprises using N-(3-methyl-1-yl) piperidine and 4-acryloyl morpholine for Michael addition reaction , then performing hydrolysis of acid to generate a novel aldehyde, making the aldehyde to carry out Wittig reactions, so that a novel morpholine amide compound is provided as a synthetic intermediate of the preparation method of the solanone. Then the compound reacts with a Grignard reagent, so that the solanone is prepared by means of the industrial method.

TERPENOIDS. SYNTHESIS OF (PLUS OR MINUS)-U- CADINENE

The starting compound 2-isopropyl- 4- carbethoxybutanal when subjected to Wittig reaction with methallylidenetriphenylphosphorane affords 2-methyl- 5- isopropyl - 7 - carbethoxy- 1,3 - heptadiene. The resulting product on Diels-Alder reaction with ethyl acrylate yields 1-methyl- 4- carbethoxy - 3 - (1 - isopropyl - 3 - carbethoxy -n - propyl) - cyclohex- lene. Cyclization of the diester followed by hydrolysis and decarboxylation gives 2-methyl- 5-oxo- 8- isopropyl - delta- l - decalene which on Wittig reaction with methylenetriphenylphosphorane furnishes (plus or minus)-U- cadinene.