23733-65-5

Usage

Uses

Used in the Food and Beverage Industry:
(R)-3-(isopropyl)-6-methylcyclohex-2-en-1-one is used as a flavoring agent for its aromatic and fruity odor, enhancing the taste and aroma of various products in the food and beverage sector.
Used in the Fragrance Industry:
(R)-3-(isopropyl)-6-methylcyclohex-2-en-1-one is also utilized in the production of fragrances, capitalizing on its pleasant and fruity scent to create appealing scents for perfumes, cosmetics, and other scented products.
Used as a Starting Material in Organic Synthesis:
Due to its unique chemical structure and reactivity, (R)-3-(isopropyl)-6-methylcyclohex-2-en-1-one serves as a starting material in the synthesis of other organic compounds, contributing to the development of new chemical entities.
Used in Pharmaceutical Applications:
(R)-3-(isopropyl)-6-methylcyclohex-2-en-1-one holds potential in the pharmaceutical industry, where its unique structure and properties can be harnessed for the development of new drugs and therapeutic agents.
Used in Agrochemical Applications:
Similarly, (R)-3-(isopropyl)-6-methylcyclohex-2-en-1-one's potential extends to the agrochemical sector, where it may be employed in the creation of novel pesticides, herbicides, or other agricultural chemicals, thanks to its specific reactivity and structural features.

InChI:InChI=1/C10H16O/c1-7(2)9-5-4-8(3)10(11)6-9/h6-8H,4-5H2,1-3H3/t8-/m1/s1

Upstream product

• 4176-04-9 (1R,4S,6S)-4,7,7-Trimethyl-bicyclo[4.1.0]heptan-3-one 
• 936-91-4 3-carene epoxide 
• 619-52-3 (1R)-menth-3-ene 
• 5113-74-6 (1R,2R,3S,4S)-2,3-epoxy-p-menthane 
• 119439-21-3 (+)-p-Menth-4-en-2-one 
• 23733-66-6 (+)-cis-Carvenol 
• 1195-92-2 (4R)-limonene 1,2-epoxide 
• 1196-31-2 (1R,4R)-(+)-isomenthone 

Relevant academic research and scientific papers

NAD(P)h-independent asymmetric C=C bond reduction catalyzed by ene reductases by using artificial co-substrates as the hydrogen donor

To develop a nicotinamide-independent single flavoenzyme system for the asymmetric bioreduction of C=C bonds, four types of hydrogen donor, encompassing more than 50 candidates, were investigated. Six highly potent, cheap, and commercially available co-substrates were identified that (under the optimized conditions) resulted in conversions and enantioselectivities comparable with, or even superior to, those obtained with traditional two-enzyme nicotinamide adenine dinucleotide phosphate (NAD(P)H)-recycling systems.

Molecular rearrangements of α-(trans)- and β-(cis)-3,4-epoxycaranes in acid media

Configuration of the oxirane ring in stereoisomeric 3,4-epoxycaranes affects the direction of their skeletal rearrangements in liquid (HSO3F-SO2FCl) and over solid (TiO2/SO42-) superacids; in the latter case, compounds postulated as intermediates in the liquid-phase process have been isolated.

REARRANGEMENT OF TERPENOIDS WITH BORON TRIFLUORIDE ETHERATE

The details of the rearrangement of some isopimaranes in the presence of boron trifluoride etherate are presented and explained.As a result of comparative studies with terpenoids in the presence of BF3, it is proposed that the complex of this Lewis acid with ketones acts as a Bronsted acid in the equilibration of double bonds.It is also suggested that natural products with the carbon skeleton of the rearrangement product should be encountered in nature.