4982-20-1

Usage

Uses

Used in Paints and Coatings Industry:
1,4-Dimethylene cyclohexane is used as a solvent to facilitate the application and drying process of paints, varnishes, and coatings. Its ability to dissolve a wide range of substances contributes to the improved performance and quality of these products.
Used in Adhesives Production:
In the adhesives industry, 1,4-dimethylene cyclohexane serves as a solvent that helps in the formulation of adhesives with desired viscosity and bonding properties, enhancing their performance in various applications.
Used in Organic Synthesis:
1,4-Dimethylene cyclohexane is utilized as a reagent in organic synthesis, where it can participate in various chemical reactions to form new compounds, contributing to the development of new chemical products and materials.
Used in Pharmaceutical Manufacturing:
As a component in the manufacturing of pharmaceuticals, 1,4-dimethylene cyclohexane plays a role in the synthesis of active pharmaceutical ingredients or in the formulation of drug products, leveraging its chemical properties to improve the efficacy and safety of medications.
Used in Agrochemicals Production:
In the agrochemicals industry, 1,4-dimethylene cyclohexane is employed in the synthesis of various agrochemical products, such as pesticides and herbicides, where it contributes to the development of effective and environmentally friendly solutions for agricultural applications.

InChI:InChI=1/C8H12/c1-7-3-5-8(2)6-4-7/h1-6H2

Upstream product

• 1871-57-4 2-chloromethyl-3-chloroprop-1-ene 
• 17616-43-2 3-iodo-2-(iodomethyl)-1-propene 
• 15456-25-4 3-methylenecyclobutanone 
• 106-99-0 buta-1,3-diene 
• 35541-76-5 1,4-bis(iodomethyl)cyclohexane 
• 105-08-8 bis-1,4-(hydroxymethyl)cyclohexane 
• 35541-78-7 cyclohexane-1,4-diyl bis(methylene) bis(4-methylbenzenesulfonate) 
• 35541-75-4 1,4-bis-(bromomethyl)cyclohexane 
• 96-22-0 pentan-3-one 
• 6308-18-5 1,4-cyclohexanedimethylene diacetate 

Downstream Products

• 106-42-3 para-xylene 
• 1595-05-7 p-butyltoluene 
• 131236-45-8 1-Methyl-4-methylene-3-propyl-cyclohexene 
• 131236-44-7 1,4-Dimethylene-2-propyl-cyclohexane 
• 131236-53-8 1-(4-Butyl-benzyl)-4-methyl-bicyclo[2.2.1]heptane 
• 131236-52-7 1-Methyl-4-(4-methylene-3-propyl-cyclohex-1-enylmethyl)-bicyclo[2.2.1]heptane 
• 84980-64-3 1-Ethenyliden-4-methylencyclohexan 
• 84980-63-2 1,4-Bis(ethenyliden)cyclohexan 
• 71707-68-1 1-Methoxymethyl-4-methylene-cyclohexane 
• 1443-80-7 4-cyanophenyl methyl ketone 
• 100-47-0 benzonitrile 
• 104-85-8 para-methylbenzonitrile 
• 143734-11-6 4-methoxy-4-methyl-1-methylenecyclohexane 

Relevant academic research and scientific papers

SYNTHESIS OF BICYCLO[2.2.2]OCTANE DERIVATIVES

Provided is a process for the preparation of certain 1,4-bicyclo[2.2.2]octane derivatives. The new synthetic procedure involves treating 1,4-dimethylene cyclohexane with an oxidizing agent in the presence of a transition metal catalyst to afford an oxo-substituted bicyclo[2.2.2]octane species. This intermediate structure can then be further derivatized. The processes of this disclosure thus affords a novel and simplified means for the commercial production of a wide variety of bicyclo[2.2.2]octane derivatives.

SYNTHESIS OF BICYCLO(2.2.2)OCTANES

Provided is a process for the preparation of certain 1,4- bicyclo[2.2.2]octane derivatives. The new synthetic procedure involves treating 1,4-dimethylene cyclohexane with an oxidizing agent in the presence of a transition metal catalyst comprising a palla

Synthesis and Structural Properties of Two Biscyclopropenes

The synthesis of two biscyclopropanes, 1 and 2, are described.Both compounds are moderately sensitive to oxygen and Lewis acids.The conformational properties of 1 were examined by dynamic 1H NMR spectroscopy.The structure of 2 was determined by low-temper

Naphthalene-catalysed lithiation of 3-chloro-2-chloromethylpropene in a Barbier-type process with carbonyl compounds

The reaction of 3-chloro-2-chloromethylpropene (1) and carbonyl compounds (2) with an excess of lithium powder in the presence of a catalytic amount of naphthalene (6%) in tetrahydrofuran at -78 to 20°C leads, after hydrolysis, to the corresponding methylenic 1,5-diols 3 in a Barbier-type process. The treatment of the crude diols 3 with 12 M. hydrochloric acid affords selectively the corresponding substituted dihydropyrans 6.

Naphthalene-catalysed lithiation of 3-chloro-2-chloromethyl-propene: A barbier-type practical alternative to the trimethylenemethane dianion

The reaction of equimolar amounts of 3-chloro-2-chloromethylpropene (2) and a carbonyl compound (3) with an excess of lithium powder and a catalytic amount (6%) of naphthalene in tetrahydrofuran at -78°C leads, after hydrolysis with water, to the correspo

Hydrogenolysis of Small Cycloalkanes, XV. - Hydrogenation of Dispirodeca-4,9-diene

On hydrogenation of the title compound 1 with Pd/C 1,4-diethylbenzene (2) is formed in 95percent yield, furthermore 1percent of cis- and 2percent of trans-1,4-diethylcyclohexane (3 and 4) as well as 2percent of 6-ethylspirooctane (15) are found.With Pt/C the intermediates 7, 12, 13, and 14 and up to 45percent of dispirodecane (17) are identified. 17 is hydrogenated with PtO2 in acetic acid to form 1,1,4,4-tetramethylcyclohexane (19).