98102-91-1

Usage

Uses

Used in Food Industry:
(+/-)-trans-2-Isopropyl-cyclohexanol is used as a flavoring agent for its minty taste, often incorporated into products such as toothpaste and chewing gum to enhance their flavor profile.
Used in Cosmetic Industry:
In the cosmetic industry, (+/-)-trans-2-Isopropyl-cyclohexanol serves as a fragrance component, adding a refreshing scent to various cosmetic products.
Used in Pharmaceutical Industry:
(+/-)-trans-2-Isopropyl-cyclohexanol is utilized in the production of pharmaceuticals, capitalizing on its unique properties to contribute to the development of medicinal compounds.
Used as a Precursor in Organic Synthesis:
(+/-)-trans-2-Isopropyl-cyclohexanol also acts as a precursor in the synthesis of other organic compounds, highlighting its versatility in organic chemistry.
Used in Health Research:
(+/-)-trans-2-Isopropyl-cyclohexanol has been studied for its potential antimicrobial and antioxidant properties, indicating its possible use in health-related applications and products.

Upstream product

• 1004-77-9 2-isopropylcyclohexanone 
• 555-31-7 aluminum isopropoxide 
• 10488-25-2 cis-2-isopropylcyclohexan-1-ol 
• 67-63-0 isopropyl alcohol 
• 67-64-1 acetone 
• 64-19-7 acetic acid 
• 64-17-5 ethanol 
• 88-69-7 2-(1-methylethyl)phenol 
• 286-20-4 cyclohexane-1,2-epoxide 
• 75-26-3 isopropyl bromide 
• 822-87-7 2-Chlorocyclohexanone 
• 96-07-1 (+/-)-trans-2-Isopropyl-cyclohexanol 

Downstream Products

• 1975-32-2 (R)-2-isopropylcyclohexanone 
• 10488-25-2 cis-2-isopropylcyclohexan-1-ol 
• 98102-89-7 (-) Trans 2-isopropyl cyclohexanol 

Relevant academic research and scientific papers

Asymmetric Induction via a Helically Chiral Anion: Enantioselective Pentacarboxycyclopentadiene Br?nsted Acid-Catalyzed Inverse-Electron-Demand Diels-Alder Cycloaddition of Oxocarbenium Ions

An enantioselective catalytic inverse-electron-demand Diels-Alder reaction of salicylaldehyde acetal-derived oxocarbenium ions and vinyl ethers to generate 2,4-dioxychromanes is described. Chiral pentacarboxycyclopentadiene (PCCP) acids are found to be effective for a variety of substrates. Computational and X-ray crystallographic analyses support the unique hypothesis that an anion with point-chirality-induced helical chirality dictates the absolute sense of stereochemistry in this reaction.

Cytochrome P450 catalyzed oxidative hydroxylation of achiral organic compounds with simultaneous creation of two chirality centers in a single C-H activation step

Regio- and stereoselective oxidative hydroxylation of achiral or chiral organic compounds mediated by synthetic reagents, catalysts, or enzymes generally leads to the formation of one new chiral center that appears in the respective enantiomeric or diastereomeric alcohols. By contrast, when subjecting appropriate achiral compounds to this type of C-H activation, the simultaneous creation of two chiral centers with a defined relative and absolute configuration may result, provided that control of the regio-, diastereo-, and enantioselectivity is ensured. The present study demonstrates that such control is possible by using wild type or mutant forms of the monooxygenase cytochrome P450 BM3 as catalysts in the oxidative hydroxylation of methylcyclohexane and seven other monosubstituted cyclohexane derivatives.

Diastereoselective reduction of cyclohexanones with diisobutylaluminium phenoxides in terms of the isoinversion principle

The diastereoselectivity of the reduction of 2-substituted cyclohexanones 1-6 with 4-substituted diisobutylaluminium phenoxides a-d has been investigated as a function of temperature. The high-temperature region is found to be dominated by hydride transfer, which is controlled by steric as well as electronic effects. However, at low temperatures the Meerwein-Ponndorf-Verley reaction gains in Importance. This phenomenon is quantified by an isoinversion relationship.