1 Trans 4 Pentylcyclohexyl 4 Iodobenzene
Iodobenzene

1 Trans 4 Pentylcyclohexyl 4 Iodobenzene

Fengxi Chemical

Specifications

HS Code

851750

Chemical Formula C17H23I
Molecular Weight 368.27
Appearance Solid (Typical for such organic compounds)
Melting Point Data may vary, needs experimental determination
Boiling Point Data may vary, needs experimental determination
Solubility In Organic Solvents Soluble in common organic solvents like toluene, dichloromethane
Solubility In Water Insoluble
Density Data may vary, needs experimental determination
Flash Point Data may vary, needs experimental determination
Stability Stable under normal conditions, but may react with strong oxidizing agents
Chemical Formula C17H23I
Molecular Weight 368.27
Appearance Solid (Typical appearance)
Solubility In Organic Solvents Soluble in common organic solvents (Typical property for this type of compound)
Purity Typically high purity in commercial products (e.g., 95%+ depending on source)
Packing & Storage
Packing 100g of 1-(trans -4 -pentylcyclohexyl)-4 -iodobenzene in a sealed, labeled chemical container.
Storage 1-(trans -4-pentylcyclohexyl)-4-iodobenzene should be stored in a cool, dry place, away from heat sources and direct sunlight. Keep it in a tightly sealed container to prevent exposure to air and moisture, which could potentially cause degradation. Store it separately from oxidizing agents and incompatible substances to avoid chemical reactions.
Shipping 1-(trans -4 -pentylcyclohexyl)-4 -iodobenzene is a chemical. Shipping should be in properly sealed, labeled containers, following hazardous materials regulations to ensure safe transportation due to its chemical nature.
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1-(trans-4-pentylcyclohexyl)-4-iodobenzene 1-(trans-4-pentylcyclohexyl)-4-iodobenzene 1-(trans-4-pentylcyclohexyl)-4-iodobenzene
General Information
Frequently Asked Questions
What are the main uses of 1- (trans-4-pentylcyclohexyl) -4-iodobenzene?
(Trans-4-cyclohexyl cyclohexyl) - 4-nitrile, which is widely used. In the field of materials science, it can be used as a raw material for the creation of special engineering plastics. These engineering plastics have high strength, high heat resistance and chemical corrosion resistance, and are often used in high-end fields such as aerospace and automobile manufacturing. In aerospace, components need to withstand extreme conditions. This material helps to make lightweight and strong parts to improve aircraft performance. In automobile manufacturing, it can be used to make high-temperature parts around the engine and body structural parts to enhance the overall strength and durability of the vehicle.
In the field of organic synthesis chemistry, (trans-4-cyclohexyl cyclohexyl) -4-nitrile is a key intermediate. Chemists can convert it into a wide range of complex organic compounds through various chemical reactions. The nitrile group of this compound can participate in many reactions, such as hydrolysis to form carboxylic acids and reduction to amines, laying the foundation for the synthesis of new drugs, pesticides and fine chemicals. When new drugs are developed, this is used as a starting material to construct a specific bioactive molecular structure through multi-step reactions, which is expected to create drugs with better efficacy and fewer side effects.
It also plays an important role in the field of liquid crystal materials. Liquid crystal materials are widely used in display technologies, such as liquid crystal displays (LCDs). ( The unique molecular structure of trans-4-cyclohexyl-cyclohexyl-4-nitrile endows the liquid crystal material with suitable phase transition temperature and good orientation characteristics, so that the LCD presents a high-resolution, high-contrast display effect, bringing people a better visual experience.
What are the physical properties of 1- (trans-4-pentylcyclohexyl) -4-iodobenzene?
(1 - (trans-4-benzylcyclohexyl) - 4-cyanobenzene, the physical properties of this substance are as follows:
It is a white crystalline solid with a pure and fine appearance. The melting point is in a specific range, about [X] ° C. This melting point characteristic is a key indicator for determining its purity and structural stability. Under normal temperature and pressure, its state is stable and it is not easy to undergo biological phase transformation due to small changes in the environment.
Furthermore, its density also has a specific value, about [X] g/cm ³, which is important for considering its distribution and behavior in different media. In terms of solubility, it exhibits good solubility in common organic solvents such as toluene and dichloromethane, and can be miscible with these solvents in a certain proportion to form a uniform solution. This property is convenient for reaction or processing as a solute in chemical synthesis and related processes. In water, its solubility is poor and almost insoluble. This property allows it to maintain a relatively independent state in the aqueous phase system, not confused with water, and can be used for the distinction and operation of substances in specific scenarios such as oil-water separation.
Its refractive index also has a corresponding value, about [X]. The refractive index reflects the degree of influence of the substance on the direction of light propagation. It has important reference significance for optical-related applications or for purity detection by optical means. These physical properties are combined to construct (a unique physical "portrait" of 1- (trans-4-benzylcyclohexyl) -4-cyanobenzene, providing a basic basis for its application in various fields of chemistry, materials science, etc.)
Note: The [X] in the above content needs to be filled in according to the actual and accurate data, and here is a schematic description.
What is the synthesis method of 1- (trans-4-pentylcyclohexyl) -4-iodobenzene?
There is currently a synthesis of (trans-4-pentylcyclohexyl) -4-cyanobenzene. The method is as follows:
First, the appropriate starting material is taken, and cyclohexanone is used as the base. After a multi-step reaction, trans-4-pentylcyclohexanol is prepared. Shilling cyclohexanone and amyl halide are catalyzed by a strong base, and nucleophilic substitution is carried out to introduce amyl groups to obtain 4-pentylcyclohexanone. This step requires mild reaction conditions to avoid side reactions and affect the yield. Then, 4-pentylcyclohexanone is reduced to 4-pentylcyclohexanol with a suitable reducing agent, such as sodium borohydride. The reaction is carried out in an alcohol solvent, and the temperature should be controlled in a moderate range, so that the reaction occurs smoothly.
After dehydration, 4-pentylcyclohexanol is converted into 4-pentylcyclohexene. Often strong acids such as sulfuric acid or p-toluenesulfonic acid are used as catalysts, and heating is used to dehydrate the alcohol to alkenes. This step should pay attention to the reaction temperature and time to prevent side reactions such as overreaction or polymerization. After 4-pentylcyclohexene is obtained, it is halogenated and added to the double bond with bromine or chlorine in a suitable solvent, such as carbon tetrachloride, to obtain 4-pentyl-1,2-dihalocyclohexane.
Then, the elimination reaction is performed, and 4-pentyl-1,2-dihalocyclohexane is treated with an alcohol solution of a strong base such as potassium hydroxide to obtain trans-4-pentylcyclohexene. This step aims to construct the trans structure, which is crucial for the precise control of the reaction conditions.
In addition, cyanobenzene is used as a raw material, and the coupling reaction with trans-4-pentylcyclohexene occurs under appropriate reaction conditions. Transition metal catalysis methods, such as palladium-catalyzed cross-coupling reactions, can be used to form (trans-4-pentylcyclohexyl) -4-cyanobenzene. Appropriate ligands need to be added to the reaction system to enhance the activity and selectivity of the catalyst. At the same time, the reaction temperature, time and proportion of reactants are carefully regulated, so that the reaction proceeds in the direction of generating the target product, and finally (trans-4-pentylcyclohexyl) -4-cyanobenzene can be obtained. After each step of the reaction, the product needs to be purified by suitable separation and purification methods, such as distillation, recrystallization, column chromatography, etc., to ensure the purity of the raw materials in the next step of the reaction and improve the efficiency and product quality of the overall synthesis.
What are the precautions for storing and transporting 1- (trans-4-pentylcyclohexyl) -4-iodobenzene?
(Trans-4-benzylcyclohexyl) - 4-nitrile This substance has many precautions during storage and transportation.
The first to bear the brunt, it is necessary to understand its chemical properties. This is an organic compound with specific chemical activities and physical properties. When storing, it should be placed in a cool, dry and well-ventilated place. Because it may be sensitive to temperature and humidity, if the environment is hot, it may deteriorate or cause chemical reactions, which may damage the quality.
Furthermore, during transportation, it is necessary to ensure that the packaging is tight and stable. The substance may be dangerous, such as packaging damage, leakage or pose a threat to the environment and personal safety. Therefore, packaging materials must meet relevant standards and be able to withstand certain external shocks and environmental changes.
In addition, storage and transportation places should be kept away from fire sources, heat sources and strong oxidants. This compound may be at risk of combustion or explosion in case of open flames, hot topics or strong oxidants. In the storage area, corresponding fire equipment and emergency treatment equipment should be equipped to prevent accidents.
At the same time, storage and transportation personnel need to be professionally trained to be familiar with the characteristics of this object and safe operating procedures. When operating, appropriate protective equipment should be worn according to regulations, such as protective gloves, glasses, etc., to avoid direct contact to prevent harm to the body.
In short, for the storage and transportation of (trans - 4 - benzylcyclohexyl) - 4 - nitrile, it is necessary to consider its chemical properties and latent risks in an all-round way, and strictly follow relevant specifications and operating procedures to ensure the safety of personnel, the environment is not damaged and the quality of goods is not affected.
What are the environmental effects of 1- (trans-4-pentylcyclohexyl) -4-iodobenzene?
The effect of (trans-4-cyclohexyl cyclohexyl) - 4-cyano on the environment is related to the role of chemical substances in natural ecology, which is an important topic.
(trans-4-cyclohexyl cyclohexyl) - 4-cyano substances, if accidentally released in the environment, will bear the brunt of affecting water ecology. In rivers, lakes and seas, it may interfere with the normal physiological functions of aquatic organisms. For example, the gills of fish may be exposed to this substance, causing gas exchange to be blocked, breathing difficulties and even death. And this substance also affects aquatic plants, or hinders their photosynthesis, destroying the ecological balance of water bodies.
The soil environment is also affected. If sewage containing this substance is used for irrigation, it may remain in the soil, changing the soil physical and chemical properties. Soil microbial communities may be inhibited, affecting the decomposition of organic matter and nutrient cycling in the soil, which is unfavorable to crop growth, resulting in reduced yield and quality.
In the atmospheric environment, although its volatilization may be limited, in specific industrial production processes, if it is not handled properly, its volatilized gaseous substances may participate in atmospheric chemical reactions. This may affect air quality, generate secondary pollutants, and endanger human health, such as irritating the respiratory tract, causing symptoms such as cough and asthma.
In addition, (trans-4-cyclohexyl cyclohexyl) -4-cyano has a certain persistence and is difficult to degrade naturally. It accumulates in the environment for a long time, is transmitted and bioenriched through the food chain, and organisms at the top of the food chain, including humans, accumulate high concentrations of this substance in the body or cause chronic health problems, such as potential carcinogenic and teratogenic risks.
To reduce its impact on the environment, industrial production needs to optimize processes and reduce emissions. At the same time, strengthen environmental monitoring, detect and deal with pollution problems in a timely manner, so as to ensure the safety of the ecological environment and human health.