15890-36-5

Basic information

• Product Name: 4-Isopropylcyclohexanol
• Synonyms: trans-4-Isopropylcyclohexanol;Ccris 8052;trans-4-(1-Methylethyl)cyclohexanol;trans-4-Isopropylcyclohexanol
• CAS NO: 15890-36-5
• Molecular Formula: C₉H₁₈O
• Molecular Weight: 142.24
• Mol File: 15890-36-5.mol
• Article Data: 9

Chemical Properties

• Melting Point: 6°C(lit.)
• Boiling Point: 94°C/5mmHg(lit.)
• Flash Point: 80.796°C
• Appearance: /
• Density: 0.9150
• Vapor Pressure: 0.068mmHg at 25°C
• Refractive Index: 1.4640 to 1.4680
• PKA: 15.30±0.40(Predicted)
• CAS DataBase Reference: 4-Isopropylcyclohexanol(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Isopropylcyclohexanol(15890-36-5)
• EPA Substance Registry System: 4-Isopropylcyclohexanol(15890-36-5)

Safety Data

• Hazardous Substances Data: 15890-36-5(Hazardous Substances Data)

Usage

General Description

4-Isopropylcyclohexanol is a chemical compound that is classified as a cyclohexanol, containing a cyclohexane ring structure with a hydroxyl group (-OH) attached to it. It also contains an isopropyl group, which consists of three carbon atoms and branching off from the cyclohexane ring. 4-Isopropylcyclohexanol is commonly used in the production of fragrances, as well as in the manufacturing of various chemical intermediates. It is also utilized as a solvent in certain applications, due to its ability to dissolve a wide range of substances. Additionally, 4-Isopropylcyclohexanol may have potential applications in the pharmaceutical industry and in the research of new drug compounds due to its unique chemical structure.

InChI:InChI=1/C9H18O/c1-7(2)8-3-5-9(10)6-4-8/h7-10H,3-6H2,1-2H3/t8-,9-

Upstream product

• 5432-85-9 4-isopropyl-cyclohexanone 
• 555-31-7 aluminum isopropoxide 
• 67-63-0 isopropyl alcohol 
• 64-17-5 ethanol 
• 950178-02-6 trans-(1S,4R)-4-isopropylcyclohex-2-enol 
• 4705-06-0 (+/-)-1r-Isopropyl-cyclohexen-⁽²⁾-ol-(4t) 
• 2158-59-0 (R)-(-)-cryptone 
• 7664-93-9 sulfuric acid 
• 99-89-8 4-Isopropylphenol 
• 4621-04-9 4-isopropylcyclohexanol 
• 33531-22-5 (+)(1S)-1r-Isopropyl-cyclohexen-⁽²⁾-ol-(4t) 
• 64-19-7 acetic acid 
• 60-29-7 diethyl ether 
• 133231-34-2 toluene-4-sulfonic acid-(trans-4-isopropyl-cyclohexyl ester) 

Downstream Products

• 98562-30-2 phthalic acid mono-(trans-4-isopropyl-cyclohexyl ester) 
• 15876-32-1 trans-4-acetoxy-1-isopropyl-cyclohexane 
• 175020-81-2 4-isopropylcyclohexyl mesylate 
• 22900-08-9 cis 4-isopropylcyclohexanol 
• 1544662-13-6 6-((cis-4-isopropylcyclohexyl)oxy)-2-methylquinoline 
• 1544662-04-5 2-bromo-6-((cis-4-isopropylcyclohexyl)oxy)naphthalene 
• 1544657-30-8 1-((6-((cis-4-isopropylcyclohexyl)oxy)naphthalen-2-yl)methyl)-4-(pyridin-2-yl)piperazine 
• 1544662-19-2 methyl 3-(1-((6-((cis-4-isopropylcyclohexyl)oxy)naphthalen-2-yl)methyl)azetidin-3-yl)cyclohexanecarboxylate 
• 1544657-44-4 3-(1-((6-((cis-4-isopropylcyclohexyl)oxy)naphthalen-2-yl)methyl)azetidin-3-yl)cyclohexanecarboxylic acid 
• 1544662-06-7 6-((cis-4-isopropylcyclohexyl)oxy)-2-naphthaldehyde 
• 94112-07-9 4-isopropyl-cyclohexanone-(2,4-dinitro-phenylhydrazone) 
• 15876-33-2 (trans-4-Isopropyl-cyclohexyl)-methyl-ether 
• 94711-12-3 3.5-dinitro-benzoic acid-(trans-4-isopropyl-cyclohexyl ester) 
• 5432-85-9 4-isopropyl-cyclohexanone 

Relevant articles and documents

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Cobalt-Nanoparticles Catalyzed Efficient and Selective Hydrogenation of Aromatic Hydrocarbons

The development of inexpensive and practical catalysts for arene hydrogenations is key for future valorizations of this general feedstock. Here, we report the development of cobalt nanoparticles supported on silica as selective and general catalysts for such reactions. The specific nanoparticles were prepared by assembling cobalt-pyromellitic acid-piperazine coordination polymer on commercial silica and subsequent pyrolysis. Applying the optimal nanocatalyst, industrial bulk, substituted, and functionalized arenes as well as polycyclic aromatic hydrocarbons are selectively hydrogenated to obtain cyclohexane-based compounds under industrially viable and scalable conditions. The applicability of this hydrogenation methodology is presented for the storage of H2 in liquid organic hydrogen carriers.

Raney Ni-Al alloy-mediated reduction of alkylated phenols in water

Raney Ni-Al alloy in a dilute aqueous alkaline solution has been shown to be a very powerful reducing agent in the hydrogenation of phenol and alkylated phenols to the corresponding cyclohexanol derivatives.