15466-94-1

Basic information

• Product Name: cis-1,3-dimethylcyclohexanol
• CAS NO: 15466-94-1
• Molecular Weight: 128.214
• Mol File: 15466-94-1.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: cis-1,3-dimethylcyclohexanol(CAS DataBase Reference)
• NIST Chemistry Reference: cis-1,3-dimethylcyclohexanol(15466-94-1)
• EPA Substance Registry System: cis-1,3-dimethylcyclohexanol(15466-94-1)

Safety Data

• Hazardous Substances Data: 15466-94-1(Hazardous Substances Data)

Upstream product

• 2207-03-6 trans-1,3-dimethylcyclohexane 
• 35023-83-7 3-ethoxy-5-methyl-cyclohex-2-enone 
• 591-24-2 3-Methylcyclohexanone 
• 103260-32-8 (+/-)-1-hydroxy-3t-methyl-cyclohexane-r-carboxylic acid methyl ester 
• 41248-16-2 (+/-)-1-hydroxy-3t-methyl-cyclohexane-r-carboxylic acid 
• 933-42-6 1-hydroxy-3-methyl-cyclohexanecarbonitrile 
• 90112-44-0 5-methyl-1-oxaspiro[2.5]octane 
• 917-64-6 methyl magnesium iodide 
• 101869-71-0 (+/-)-1-hydroxymethyl-cis-3-methylcyclohexanol 
• 18006-13-8 methyltriisopropoxytitanium(IV) 
• 917-54-4 methyllithium 
• 2747-38-8 methyltrichlorotitanium 
• 7214-50-8 5-methylcyclohex-2-en-1-one 
• 75-16-1 methylmagnesium bromide 

Downstream Products

• 638-04-0 cis-1,3-dimethylcyclohexane 
• 2207-03-6 trans-1,3-dimethylcyclohexane 
• 128749-93-9 1r.3c-dimethyl-cyclohexanediol-(1.3t) 
• 101869-68-5 (+/-)-1r.3t-dimethyl-cyclohexanediol-(1.3c) 

Relevant articles and documents

Selective C-H bond hydroxylation of cyclohexanes in water by supramolecular control

A new approach for selective hydroxylation of non-activated cyclohexanes using dioxirane generated in situ in water through supramolecular control has been developed. Using β-CD and γ-CD as the supramolecular hosts, selective hydroxylation of cyclohexane substrates, including trans/cis-1,4-, 1,3-and 1,2-dimethylcyclohexanes and trans/cis-decahydronaphthalene, was achieved in up to 54% yield in water. Furthermore, site-selective C-H bond hydroxylation of (+)-menthol was achieved by obstructing the approach of dioxirane to the C-H bond with higher steric hindrance through inclusion complexation with β-CD and γ-CD in water.

Facial Stereoselectivity of Two-Step Additions Initiated by Electrophilic Halogens to Methylenecyclohexanes. A Comparison with Epoxidation

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Diastereoselective Addition of Organoytterbium Reagents to Carbonyl Substrates

Organoytterbium reagents, prepared by the addition of organolithiums or organomagnesiums to ytterbium(III) triflate, react in a highly diastereoselective fashion with a variety of chiral aldehydes and ketones.