24434-24-0

Usage

Chemical structure

Cyclohexanol derivative

Explanation

The compound is derived from cyclohexanol, which is a type of alcohol containing a cyclohexane ring with a hydroxyl group attached.

Explanation

The compound contains three functional groups a hydroxyl group (-OH), an ethyl group (-CH2CH3), and a cyclohexyl group (a six-membered ring with two CH2 groups attached).

Explanation

Due to its pleasant smell, 1-[2-(1-hydroxycyclohexyl)ethyl]cyclohexan-1-ol is used in the production of fragrances and perfumes to provide a desirable scent.

Explanation

The compound can be used as a starting material or intermediate in the synthesis of various other organic compounds, making it a versatile building block in chemical reactions.

Explanation

The compound may have potential uses in the development of products in the pharmaceutical and cosmetic industries, although specific applications are not mentioned in the provided material.

Explanation

Due to its various applications in different industries, 1-[2-(1-hydroxycyclohexyl)ethyl]cyclohexan-1-ol is considered a valuable chemical compound with significant industrial and commercial importance.

Functional groups

Hydroxyl group, ethyl group, and cyclohexyl group

Application in fragrances and perfumes

Pleasant odor

Precursor in organic synthesis

Synthesis of other organic compounds

Potential applications

Pharmaceutical and cosmetic industries

Industrial and commercial uses

Valuable chemical compound

Upstream product

• 23708-48-7 pentamethylenebis(magnesium bromide) 
• 123-25-1 succinic acid diethyl ester 
• 78-54-6 1,2-di(1-hydroxycyclohexyl)acetylene 
• 4301-15-9 ethynyldimagnesium dibromide 
• 108-94-1 cyclohexanone 
• 185-18-2 1-Oxaspiro<5.5>nonane 
• 106-93-4 ethylene dibromide 
• 195154-34-8 1-(2-Phenylsulfanyl-ethyl)-cyclohexanol 
• 1940-19-8 1-vinylcyclohexanol 
• 67-56-1 methanol 
• 64-17-5 ethanol 
• 10035-10-6 hydrogen bromide 
• 67-63-0 isopropyl alcohol 
• 74-86-2 acetylene 

Relevant academic research and scientific papers

TiCl4/Mg/BrCH2CH2Br Reagent System: A 1,2-Diorganometallic Equivalent

1,2-Diorganometallic species generated utilizing the TiCl4/Mg/BrCH2CH2/Br reagent system reacts with ketones to give the corresponding 1,4-diols and/or 1,2-diols in moderate yields.

NEW BIFUNCTIONAL (METH)ACRYLATE COMPOUND AND POLYMER

Provided is a compound that can be used for a resin for a resist having excellent sensitivity, resolution, and etching resistance, or the like, by a compound represented by the following formula (1): (wherein R1 represents a hydrogen atom or a

Synthesis and Applications of Tetrahydrofuran-Stable Substituted (3-Lithioxyalkyl)- and (4-Lithioxyalkyl)lithiums, Modified with Magnesium 2-Ethoxyethoxide

Substituted hydroxyalkyl phenyl sulfides 3 have been synthesized from the corresponding allylic or homoallylic alcohols 2. Regiospecific cleavage of the C - SPh bond of the sulfides 3 by lithium dispersion in tetrahydrofuran (THF) led to the synthesis of substituted (3-lithioxyalkyl)- and (4-lithioxyalkyl)lithiums 4, most of which share the ω carbon with a carbocyclic ring. The organolithiums were modified with magnesium 2-ethoxyethoxide in order to suppress their reactivity toward THF cleavage, thus offering the advantage of preparing storable ethereal solutions of certain types of (lithioxyalkyl)lithiums. This strategy appears to be of rather broad scope. The functionalized organolithiums prepared in this way react normally with electrophilic reagents with yields in the range 35-55%. Thus, carboxylations of 4 yielded lactones 5, some of which are natural products, while reactions of 4 with benzophenone and cyclic ketones yielded 1,4- and 1,5-diols 6 and 7, respectively.

γ-Lithioalkoxides via Reductive Lithiation of Oxetanes by Aromatic Radical Anions

Oxetanes are cleaved at 0 deg C in tetrahydrofuran by lithium 4,4'-di-tert-butylbiphenylide, giving lithium γ-lithioalkoxides which can provide 2-substituted tetrahydrofurans by trapping with aldehydes and ketones followed by acid cyclization of the resulting 1,4-diols; the cuprates of these dianions undergo conjugate addition and nucleophilic substitution reactions.