586-82-3 Usage
Description
4-(isopropyl)-1-methylcyclohex-3-en-1-ol is an organic compound that is found in various natural sources such as camphor essential oil, grapefruit juice, mandarin, lemon and lime peel oil, ginger, cognac, white wine, cocoa, tea, plum, cardamom, Roman chamomile oil, and mastic gum fruit oil. It has a dry, woody, and somewhat musty odor, and is considered an undesirable component of commercial terpineol due to its chemical properties.
Uses
Used in Flavor and Fragrance Industry:
4-(isopropyl)-1-methylcyclohex-3-en-1-ol is used as a flavoring agent for its distinct dry, woody, and musty odor. It adds depth and complexity to the fragrances and flavors in various products, such as perfumes, colognes, and food items.
Used in Essential Oils:
In the essential oil industry, 4-(isopropyl)-1-methylcyclohex-3-en-1-ol is used for its unique scent profile, which can enhance the aroma of essential oils derived from plants and fruits.
Used in the Beverage Industry:
4-(isopropyl)-1-methylcyclohex-3-en-1-ol is used as a flavor enhancer in the beverage industry, particularly in wines, cognacs, and other alcoholic drinks, to provide a richer and more complex taste.
Used in the Cosmetic Industry:
In the cosmetic industry, 4-(isopropyl)-1-methylcyclohex-3-en-1-ol is used as a fragrance ingredient in various personal care products, such as lotions, creams, and perfumes, to create a pleasant and long-lasting scent.
Used in the Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, due to its presence in various natural sources and unique chemical properties, 4-(isopropyl)-1-methylcyclohex-3-en-1-ol could potentially be used in the pharmaceutical industry for the development of new drugs or as a component in drug formulations. Further research would be required to explore its potential applications in this field.
Check Digit Verification of cas no
The CAS Registry Mumber 586-82-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,8 and 6 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 586-82:
(5*5)+(4*8)+(3*6)+(2*8)+(1*2)=93
93 % 10 = 3
So 586-82-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H18O/c1-8(2)9-4-6-10(3,11)7-5-9/h4,8,11H,5-7H2,1-3H3
586-82-3Relevant articles and documents
Synthesis of (1S,4R)-4-isopropyl-1-methyl-2-cyclohexen-1-ol, the aggregation pheromone of the ambrosia beetle Platypus quercivorus, its racemate, (1R,4R)- and (1S,4S)-isomers
Mori, Kenji
, p. 2133 - 2142 (2007/10/03)
(S)-Perillyl alcohol was converted to (R)-cryptone (91.5-93% ee) in six steps, which was then treated with methyllithium to give (1S,4R)-4-isopropyl-1-methyl-2-cyclohexen-1-ol, the aggregation pheromone of the ambrosia beetle Platypus quercivorus. The racemic pheromone was also prepared by methylation of (±)-cryptone. Both (1R,4R)- and (1S,4S)-isomers (98% ee) of the pheromone were synthesized from the enantiomers of dihydrolimonene oxide.
HYDROGENOLYSE EN PHASE LIQUIDE SUR Pd/C DES EPOXYDES DU CARVOMENTHENE ET DU LIMONENE
Accrombessi, G.,Geneste, P.,Olive, J.-L.,Pavia, A. A.
, p. 3135 - 3140 (2007/10/02)
Hydrogenolysis over Pd/C of cis and trans epoxides of carvomenthene and limonene give a mixture of hydrocarbons, secondary and tertiary alcohols, and ketones in proportions dependent upon the nature of the starting material.In the limonene epoxides, the extracyclic double bond plays an important role in the opening of the oxirane ring through a common unsaturated tertiary alcohol intermediate by double bond migration, hydrogenation of which leads to the products.For the carvomenthene epoxides the results are similar to those found in the 4-t-butyl series with competition between cis addition and trans addition of hydrogen.The presence of the isopropenyl group leads to slower reaction rates in comparison with t-butyl analogues.
