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What is the main use of 4- {4- [2- (4-ethylcyclohexyl) ethyl] cyclohexyl} -1,2-difluorobenzene
4- {4- [2- (4-ethylcyclohexyl) ethyl] cyclohexyl} -1,2-dichloroethylene, its main use is in the field of organic synthesis, often as a key intermediate in the construction of a variety of complex organic compounds.
The unique cyclic and halogenated vinyl parts in the structure of this compound give it special reactivity and selectivity. It can be used by various chemical reactions, such as nucleophilic substitution, addition, etc., to introduce and modify different functional groups for the synthesis of high value-added organic products related to medicine, pesticides and materials science.
In the field of medicine, it can be used as a raw material for structural optimization of lead compounds, and chemically modified to obtain new drug molecules with specific biological activities and pharmacological properties; in the field of pesticide research and development, it can be used to synthesize pesticide ingredients with high insecticidal, bactericidal or herbicidal properties. In the field of materials science, it can be used to prepare functional polymer materials, such as polymers with special optical and electrical properties, providing an important basis for material modification and innovation.
Cover Due to its special structure, it exhibits unique chemical behavior in organic synthesis reactions, providing a key way to create diverse and high-value organic products, and plays an important role in many fields.
What are the physical properties of 4- {4- [2- (4-ethylcyclohexyl) ethyl] cyclohexyl} -1,2-difluorobenzene
4 - {4 - [2 - (4 - ethylcyclohexyl) ethyl] cyclohexyl} - 1,2 - difluorobenzene is an organic compound. Its physical properties are as follows:
This compound is usually liquid at room temperature. Due to the presence of fluorine atoms, it has certain unique properties. In terms of melting boiling point, due to the presence of van der Waals forces between molecules and the influence of fluorine atoms, the melting boiling point will be in a specific range, but the specific value needs to be accurately determined by experiments. Generally, the introduction of fluorine atoms will change the intermolecular forces, and its boiling point may be increased compared to compounds with similar structures but no fluorine.
In terms of solubility, it is difficult to dissolve in water, because the organic substance as a whole is non-polar or weakly polar, while water is a polar solvent. According to the principle of "similar miscibility", the two are insoluble. However, it is easily soluble in common organic solvents, such as ether, chloroform, toluene, etc. These organic solvents are similar to its polarity and can dissolve each other through intermolecular forces.
In terms of density, it will be slightly larger than water, and the specific value also needs to be determined by experimental measurement. It can be used as an important intermediate in the field of chemical synthesis to prepare materials or drugs with special properties. Its physical properties have an important impact on the conditions of related reactions and the properties of products.
Are the chemical properties of 4- {4- [2- (4-ethylcyclohexyl) ethyl] cyclohexyl} -1,2-difluorobenzene stable?
4 - {4 - [2 - (4 - ethylcyclohexyl) ethyl] cyclohexyl} - 1,2 - difluorobenzene is an organic compound. Whether its chemical properties are stable needs to be analyzed from many aspects.
From the molecular structure, the benzene ring has a conjugated system, which enhances the molecular stability. The alkyl and cyclohexyl groups connected to the benzene ring further consolidate the molecular stability through the sigma-π superconjugation effect. The introduction of fluorine atoms, due to the high electronegativity of fluorine and the high bond energy of C-F, makes the molecular structure stable.
However, in terms of reactivity, although the whole is relatively stable, under certain conditions, the benzene ring can undergo electrophilic substitution reactions, such as with halogens, nitric acid, sulfuric acid and other electrophilic reagents. Alkyl side chains can undergo oxidation, halogenation and other reactions.
In normal environments, without special conditions and reagents, 4 - {4- [2- (4-ethylcyclohexyl) ethyl] cyclohexyl} -1,2 - difluorobenzene has relatively stable chemical properties. However, under extreme conditions such as high temperature, strong acid and base, and strong oxidizing agents, chemical reactions may occur and the stability may be destroyed.
What is the production process of 4- {4- [2- (4-ethylcyclohexyl) ethyl] cyclohexyl} -1,2-difluorobenzene
4- {4- [2- (4-ethylcyclohexyl) ethyl] cyclohexyl} -1,2-dichloroethylene is an organic compound, and its preparation process is as follows:
First construct a structural fragment containing 4- {4- [2- (4-ethylcyclohexyl) ethyl] cyclohexyl} with suitable starting materials. It can be achieved by multi-step reaction, such as the use of halogenated hydrocarbons and metal-organic reagents (such as Grignard reagents), the gradual introduction of ethyl and corresponding substituents on cyclohexyl to build a specific carbon chain skeleton.
After the desired cyclic and substituent structures are formed, halogenation reactions can be used for the introduction of the 1,2-dichloroethylene moiety. With a suitable olefin as the substrate, under appropriate reaction conditions, an addition reaction occurs with a halogen (such as chlorine gas), so that two chlorine atoms are introduced at the double bond position, thereby forming the 1,2-dichloroethylene structure.
The reaction process requires strict control of the reaction conditions, such as temperature, reactant ratio, reaction time, etc. Precise control of temperature is essential for the reaction selectivity and yield. Too high or too low temperature may lead to the occurrence of side reactions. The proportion of reactants also needs to be precisely adjusted to ensure that each step of the reaction proceeds as expected and avoid waste of raw materials or impurity of the product. At the same time, selecting the appropriate catalyst and reaction solvent can also promote the reaction, improve the reaction efficiency and product purity. The whole preparation process needs to follow the standard operation procedure of organic synthesis to obtain high-purity 4 - {4- [2- (4-ethylcyclohexyl) ethyl] cyclohexyl} -1,2 -dichloroethylene products.
What is the market price of 4- {4- [2- (4-ethylcyclohexyl) ethyl] cyclohexyl} -1,2-difluorobenzene
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