96-07-1

Basic information

• Product Name: 2-isopropylcyclohexan-1-ol
• Synonyms: 2-isopropylcyclohexan-1-ol;2-Isopropylcyclohexanol;Ai3-17386;Cyclohexanol, 2-(1-methylethyl)-;Einecs 202-474-6;2-propan-2-ylcyclohexan-1-ol
• CAS NO: 96-07-1
• Molecular Formula: C₉H₁₈O
• Molecular Weight: 142.23862
• EINECS: 202-474-6
• Mol File: 96-07-1.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 203.1°Cat760mmHg
• Flash Point: 80.8°C
• Appearance: /
• Density: 0.914g/cm³
• Vapor Pressure: 0.0684mmHg at 25°C
• Refractive Index: 1.466
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 2-isopropylcyclohexan-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-isopropylcyclohexan-1-ol(96-07-1)
• EPA Substance Registry System: 2-isopropylcyclohexan-1-ol(96-07-1)

Safety Data

• Hazardous Substances Data: 96-07-1(Hazardous Substances Data)

Usage

General Description

2-Isopropylcyclohexan-1-ol, also known as 2-isopropyl-1-cyclohexanol, is a chemical compound with the molecular formula C10H20O. It is a clear, colorless liquid with a slightly sweet odor. This chemical is used as an intermediate in the production of fragrances, flavors, and pharmaceuticals. It is also used as a solvent and in the manufacturing of other organic compounds. 2-Isopropylcyclohexan-1-ol is flammable and should be handled with care, using appropriate safety precautions during storage and handling. 2-isopropylcyclohexan-1-ol is not known to be a significant environmental pollutant or to have serious health effects, but should still be used with caution in a controlled industrial setting.

InChI:InChI=1/C9H18O/c1-7(2)8-5-3-4-6-9(8)10/h7-10H,3-6H2,1-2H3

Upstream product

• 88-69-7 2-(1-methylethyl)phenol 
• 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 
• 822-87-7 2-Chlorocyclohexanone 
• 286-20-4 cyclohexane-1,2-epoxide 
• 75-26-3 isopropyl bromide 

Downstream Products

• 10488-25-2 cis-2-isopropylcyclohexan-1-ol 
• 1004-77-9 2-isopropylcyclohexanone 
• 938-02-3 1-hydroxy-c-2-isopropyl-r-1-cyclohexanecarbonitrile 
• 938-02-3 1-hydroxy-c-2-isopropyl-r-1-cyclohexanecarbonitrile 
• 98102-89-7 (-) Trans 2-isopropyl cyclohexanol 
• 92729-19-6 2-Isopropyl-1-phenyl-cyclohexanol 
• 92650-76-5 6-Isopropyl-1-phenyl-cyclohexen-⁽¹⁾ 
• 98102-91-1 (R)(+)-1r-Isopropyl-cyclohexanol-(2t) 
• 1975-32-2 (R)-2-isopropylcyclohexanone 
• 1236357-39-3 p-tolyl-carbamic acid 2-isopropyl-cyclohexyl ester 

Relevant articles and documents

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.

Stereoselective hydrogenation of simple ketones catalyzed by ruthenium(II) complexes

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