92485-95-5

Usage

Uses

Used in Fragrance Industry:
1(2H)-Naphthalenone, octahydro-8-hydroxy-8a-methyl-, (4aalpha,8alpha,8 aalpha)is used as a fragrance ingredient for its distinct and appealing scent. It is commonly added to perfumes, cosmetics, and household products to provide a pleasant aroma and enhance the overall sensory experience for consumers.
Used in Pharmaceutical Industry:
Due to its unique chemical structure and properties, 1(2H)-Naphthalenone, octahydro-8-hydroxy-8a-methyl-, (4aalpha,8alpha,8 aalpha)may have potential applications in the pharmaceutical industry. It could be utilized in the development of new drugs or as a key component in the synthesis of various medicinal compounds.
Used in Research:
1(2H)-Naphthalenone, octahydro-8-hydroxy-8a-methyl-, (4aalpha,8alpha,8 aalpha)-'s distinct structure and stereoisomerism make it an interesting subject for research in the field of chemistry. It can be studied to better understand the properties and behavior of similar compounds, potentially leading to the discovery of new applications and uses in various industries.

Upstream product

• 127708-29-6 (1S,4R,6R,10R)-10 hydroxy-1-methyl-4-(trimethylsilyl)bicyclo<4.4.0>decan-2-one 
• 930-68-7 cyclohexenone 
• 147895-12-3 methyl 4-(3-oxocyclohexyl)butanoate 
• 91253-59-7 3-(4-pentenyl)cyclohexan-1-one 
• 83406-41-1 cis-1-methylbicyclo<4.4.0>decane-2,10-dione 
• 83406-42-2 9-methyl-trans-decalin-1,8-dione 
• 24037-80-7 8-hydroxy-3,4,4a,5,6,7-hexahydronaphthalen-1(2H)-one 
• 113116-57-7 3-(4-oxobutyl) cyclohexanone 
• 100315-21-7 ethyl 4-(3-oxocyclohexyl)butanoate 
• 147932-61-4 4-(3-oxo-cyclohexyl)-butyric acid 
• 127708-28-5 (1S,4R,6R)-1-methyl-4-(trimethylsilyl)bicyclo<4.40>decane-2,10-dione 

Relevant academic research and scientific papers

Preparative Bioorganic Chemistry, XVII. Reduction of a Prochiral Diketone, 9-Methyl-trans-decalin-1,8-dione, with Baker's Yeast

Reduction of 9-methyl-trans-decalin-1,8-dione (1) with baker's yeast affords (8S,9R,10R)-8-hydroxy-9-methyl-trans-1-decalone (8) as the major product in 47percent yield.Its (8S,9S,10S)-isomer (9, 14percent yield) and (1S,8S)-9-methyl-trans-1,8-diol (10, 7percent yield) are obtained as minor products.Baker's yeast cannot reduce 9-methyl-cis-decalin-1,8-dione (2). Key Words: Asymmetric reduction / Baker's yeast / Yeast / Saccharomyces cerevisia / Enzymes / trans-1-Decalone derivatives / trans-1,8-Decalindione derivatives

A new enantioselective approach to the bicyclo[4.4.0]decane and bicyclo[4.3.0]nonane systems

Highly diasteroselective routes to cis-fused bicyclo[4.4.0]decane-2,10-diones and bicyclo[4.3.0]nonane-2,9-diones from 5-trimethylsilyl-2-cyclohexen-1 -one (1a) and its 3-methyl derivative were established by utilizing an annulation with Ω-(alkoxycarbonyl

PREPARATION OF BYCYCLOOCTANE-2,8-DIONE- AND DECALIN-1,8-DIONE-DERIVATIVES

Alkylation of bicyclooctane-2,8-dione (1), which is prepared by a modification of the procedure described in the literature, gives the methyl- and propynyl-derivatives 6 and 7 (Scheme 1).In addition to the method described previously (Scheme 2), 9-