14203-64-6

Usage

Uses

Used in Pharmaceutical Industry:
1,4-Dioxaspiro[4.5]dec-6-en-8-one, 7,9,9-trimethylis used as an intermediate in the synthesis of Tabanone (T003450) for its potential natural antioxidant properties. Tabanone is found in the oils of Trifolium Pratense L., a plant species known for its medicinal properties. The antioxidant properties of Tabanone make it a promising candidate for the development of new drugs and therapies targeting oxidative stress-related diseases.
Used in Chemical Industry:
1,4-Dioxaspiro[4.5]dec-6-en-8-one, 7,9,9-trimethylis also used as a key building block in the synthesis of various organic compounds, particularly those with complex ring structures. Its unique spirocycle structure and functional groups make it a valuable component in the development of novel molecules with potential applications in various fields, such as materials science, agrochemistry, and pharmaceuticals.

Upstream product

• 1125-21-9 2,6,6-trimethyl-2-cyclohexene-1,4-dione 
• 107-21-1 ethylene glycol 
• 99708-51-7 2,6,6-trimethyl-2-hydroxy-4,4-(ethylenedioxy)cyclohexanone 
• 65339-06-2 7,9,9-Trimethyl-1,4-dioxaspiro<4.5>dec-7-ene 
• 78-59-1 3,5,5-Trimethylcyclohex-2-en-1-one 

Downstream Products

• 57685-64-0 4-[3-(1-Ethoxy-ethoxy)-butyl]-4-hydroxy-3,5,5-trimethyl-cyclohex-2-enone 
• 141885-56-5 5-(1'-hydroxy-2',6',6'-trimethyl-4'-oxo-2'-cyclohexen-1'-yl)-3-methylbenzoic acid 
• 60047-19-0 4-(3-hydroxybutyl)-3,5,5-trimethylcyclohex-2-enone 
• 54265-21-3 4-[3-Hydroxy-but-(E)-ylidene]-3,3,5-trimethyl-cyclohexanone 
• 54265-20-2 4-(3-Hydroxy-but-1-enylidene)-3,5,5-trimethyl-cyclohex-2-enone 
• 23526-45-6 6,9-dihydroxymegastigma-4,7-dien-3-one 
• 13215-88-8 4-(But-2-enylidene)-3,5,5-trimethylcyclohex-2-enone 
• 52103-92-1 4-Hydroxy-3,4,5,5-tetramethyl-2-cyclohexen-1-on 
• 38818-55-2 4-<(E)-Buta-1,3-dienyl>-3,5,5-trimethylcyclohex-2-enone 
• 5298-13-5 (E)-4-<(Z)-But-2-enylidene>-3,5,5-trimethylcyclohex-2-enone 
• 5164-78-3 (E)-4-<(E)-But-2-enylidene>-3,5,5-trimethylcyclohex-2-enone 
• 5164-79-4 (Z)-4-<(Z)-But-2-enylidene>-3,5,5-trimethylcyclohex-2-enone 
• 5492-79-5 (Z)-4-<(E)-But-2-enylidene>-3,5,5-trimethylcyclohex-2-enone 
• 6901-96-8 abscisic acid methylester 

Relevant academic research and scientific papers

An efficient synthesis of the plant hormone abscisic acid

An efficient stereospecific synthesis of the plant hormone (RS)-abscisic acid from the readily available 4-oxoisophorone, trimethylsilylacetylene and ethyl but-2-ynoate, is described.

Structure-Odor Correlation, XX. Synthesis and Olfactory Properties of the "Irone-Type Homolog" of Megastigmatrien-3-one

rac-2-Methylmegastigma-4,6,8-trien-3-one (11), the irone-type homolog of the important aroma component megastigmatrien-3-one (1), was synthesized starting from 4-oxoisophorone (2) via 2-methyl-4-oxoisophorone (7) and the ynediol 10 and additionally by met

Structure-Odor Correlation, XIII. - Synthesis and Olfactive Properties of Megastigmatrienone Analogues

The key compound 9 was readily prepared in larger quantities by an improvement of a known procedure.Addition of carbanions to the unprotected ketone 9 gives the hydroxy ketones 16 - 21 via the acetals 10 - 15.Dehydration of 16 - 20 furnishes the dienones

Technische Verfahren zur Synthese von Carotinoiden und verwandten Verbindungen aus 6-Oxo-isophoron. VI. Synthese von Rhodoxanthin und (3RS,3'RS)-Zeaxanthin; Zugaenge zur C15-Ringkomponente ueber 3-Oxo-jonon-Derivative

The C15-ring component 4, key intermediate of a new scheme for the synthesis of rhodoxanthin (1) and (3RS,3'RS)-zeaxanthin (3), has been synthesized starting from 6-oxo-isophorone (7) via 3-oxo-cyclocitral and 3-oxo-ionone derivatives.