4-Chloromethyl-1-Cyclohexyl-2-(Trifluoromethyl)Benzene
Linshang Chemical
HS Code |
508719 |
Chemical Formula | C15H16ClF3 |
Molecular Weight | 288.74 |
Appearance | Typically a colorless to light - colored liquid |
Boiling Point | Data may vary, around a certain temperature range related to its molecular structure |
Melting Point | Specific melting point value related to its crystal lattice |
Density | A value indicating mass per unit volume |
Solubility In Water | Low solubility due to non - polar nature |
Solubility In Organic Solvents | Good solubility in common organic solvents like toluene, dichloromethane |
Vapor Pressure | Characteristic vapor pressure at a given temperature |
Flash Point | Value representing the temperature at which it can form an ignitable vapor - air mixture |
As an accredited 4-Chloromethyl-1-Cyclohexyl-2-(Trifluoromethyl)Benzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
Packing | 500g of 4 - chloromethyl - 1 - cyclohexyl - 2 - (trifluoromethyl)benzene in sealed chemical - grade bottle. |
Storage | Store 4 - chloromethyl - 1 - cyclohexyl - 2 - (trifluoromethyl)benzene in a cool, dry, well - ventilated area, away from heat sources and open flames. Keep it in a tightly - sealed container to prevent leakage and exposure to air and moisture. Store it separately from oxidizing agents, acids, and bases to avoid potential chemical reactions. |
Shipping | 4 - chloromethyl - 1 - cyclohexyl - 2 - (trifluoromethyl)benzene is shipped in accordance with chemical transport regulations. It's carefully packaged to prevent leakage, transported by approved carriers ensuring safety during transit. |
Competitive 4-Chloromethyl-1-Cyclohexyl-2-(Trifluoromethyl)Benzene prices that fit your budget—flexible terms and customized quotes for every order.
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As a leading 4-Chloromethyl-1-Cyclohexyl-2-(Trifluoromethyl)Benzene supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.
When creating new drug molecules, this compound often acts as a key intermediate. Because its structure contains special functional groups, such as chloromethyl, trifluoromethyl and cyclohexyl, these functional groups give it unique chemical properties and reactivity. The existence of chloromethyl can induce nucleophilic substitution reactions, introduce different groups, expand the complexity of molecular structures, and provide the possibility of constructing specific active structures in drug development.
In the field of materials science, it also has its uses. Due to the characteristics of trifluoromethyl, it can improve the physical and chemical properties of materials, such as enhancing the corrosion resistance of materials and improving their thermal stability. Materials made from this compound or in fields with strict material performance requirements such as aerospace and electronic devices have made a name for themselves.
In addition, it can also be seen in the field of pesticide synthesis. With its special structure, pesticide products with high insecticidal and bactericidal activities can be designed and synthesized, contributing to the pest control of agricultural production. In conclusion, 4-chloromethyl-1-cyclohexyl-2 - (trifluoromethyl) benzene has important uses in many fields such as organic synthesis, drug development, materials science, and pesticide synthesis, and is indeed an important compound in the field of organic chemistry.
First of all, discuss its physical state. Under normal temperature and pressure, it is mostly in a liquid state due to the characteristics of intermolecular forces. This liquid state gives it fluidity, and it has unique performance when transporting, storing and participating in reactions.
Melting point and boiling point. The melting point is low, so that it can be melted into a liquid state under relatively mild conditions, which is conducive to processing. The boiling point is higher, indicating that a higher temperature is required to convert it into a gaseous state. This is because the molecule contains chlorine, fluorine and other halogen atoms, which increases the intermolecular force and causes the boiling point to rise.
Looking at its solubility, this compound is slightly special. Because it contains trifluoromethyl, it has strong hydrophobicity and is extremely difficult to dissolve in water, but it has good solubility in organic solvents such as dichloromethane, chloroform, toluene, etc. The characteristics of this solubility have a significant impact on its separation, purification and application in organic synthesis reaction systems.
Again, the density is higher than that of common organic solvents and slightly higher than that of water. This property is used in liquid-liquid separation operations, or can be distinguished from other substances by density differences.
In terms of its volatility, although it is not a highly volatile substance, it is still in its liquid state and has a certain vapor pressure. Under open system or heating conditions, some volatilization will still escape. When using and storing, care should be taken to prevent loss due to volatilization or safety issues.
In addition, its appearance may be colorless to light yellow transparent liquid. This color and transparency are also its physical characteristics, which can provide clues for identification and quality judgment.
All these physical properties are interrelated and jointly determine the application and operation specifications of 4-chloromethyl-1-cyclohexyl-2 - (trifluoromethyl) benzene in the chemical industry, medicine and other fields.
One method is to take the benzene derivative containing cyclohexyl first, so that it can be substituted with the reagent containing trifluoromethyl under appropriate reaction conditions. This reaction requires careful selection of catalysts to increase the rate and selectivity of the reaction. Commonly used catalysts, or metal salts, can effectively combine the two in a mild reaction environment to obtain benzene intermediates containing trifluoromethyl and cyclohexyl.
Then, for this intermediate, if you want to introduce chloromethyl, you can use halogenated reagents and methyl-containing reagents. In a specific reaction solvent, the halogenated reagent is substituted with a specific position on the intermediate, and the methyl is skillfully converted to chloromethyl. This process requires fine regulation of the reaction temperature and time to prevent over-halogenation or side reactions.
There is another method, which can be reversed. Introducing chloromethyl on the benzene ring first, the commonly used method is to react with chloromethylated reagents and benzene derivatives. Such reaction conditions may be more severe, but if properly controlled, chloromethyl can also be introduced accurately. Then, the cyclohexylation reagent is reacted with the benzene derivative containing chloromethyl, followed by the reagent containing trifluoromethyl for substitution, and the structure of the target compound is gradually constructed.
These two methods have their own advantages and disadvantages. The former first introduces a larger group, which is conducive to the positioning and control of the subsequent reaction, but requires a high catalyst; the latter although the steps are slightly complicated, but the conditions of each step of the reaction are controlled, or more flexible. To choose the optimal method, it is necessary to comprehensively consider many factors such as the availability of raw materials, the cost of the reaction, the yield, and the purity of the product. The way of synthesis is like exploring a hidden path, and it is necessary to be cautious and delve into the state to obtain a pure target product.
First, because of its chemical activity, avoid high temperature. High temperature is easy to initiate chemical reactions, causing material deterioration, or dangerous. In case of hot topic, or decomposition, release harmful gases, damage the environment and human body. Therefore, it is appropriate to store in a cool place and control the temperature within a reasonable range.
Second, waterproofing is also important. Water may react with the compound, affecting its quality. Some organic compounds hydrolyze in water, destroying their structure and losing their original properties. When stored, the environment must be kept dry. Desiccant can be used to absorb moisture, and the packaging is tight to prevent moisture from entering.
Third, this compound may be toxic and corrosive, and it is harmful to contact. When stored, it should be kept away from food, medicine and daily necessities to avoid pollution. And it should be stored in a place beyond the reach of children to prevent accidental ingestion or contact.
Fourth, the choice of packaging materials is also critical. It is necessary to choose those that are compatible with it and do not react with it. Such as plastic and glass containers, choose according to the characteristics of the compound. Glass is stable, transparent and easy to perceive, but fragile; plastics are light and impact-resistant, and some plastics interact with compounds. Consider carefully when selecting.
Fifth, clear labels are indispensable. The name, characteristics, hazards and emergency treatment methods of the detailed compound. Once something happens, people can quickly know the details and take correct measures to reduce the damage.
In short, 4-chloromethyl-1-cyclohexyl-2 - (trifluoromethyl) benzene must be stored according to its characteristics, and various points must be observed to ensure the safety of its quality, human body and environment.
If this substance enters the natural environment, the first to bear the brunt is the aquatic ecosystem. Because of its hydrophobicity, it is easy to absorb water particles and then sink to the bottom. This can affect benthic organisms, or cause their physiological dysfunction and stunted development. And its degradation in water is slow, long-term accumulation, or the water ecological balance is destroyed, and the survival and reproduction of aquatic organisms such as fish and shellfish are threatened.
In the soil environment, it can be adsorbed by soil particles. Due to its stable structure, it is difficult for microorganisms to decompose it rapidly. Over time, it may change the physical and chemical properties of the soil, affecting the structure and function of the microbial community in the soil. When plant roots ingest nutrients from the soil, they may also absorb this substance, affecting the growth and development of plants, or even passing through the food chain, endangering higher trophic organisms.
In the atmospheric environment, although its volatility is not very high, under certain conditions, it may evaporate into the atmosphere. In the atmosphere, it may participate in photochemical reactions, generate other harmful products, affect air quality, and cause damage to the respiratory system of humans and organisms.
In addition, the toxicity of 4-chloromethyl-1-cyclohexyl-2 - (trifluoromethyl) benzene may interfere with the nervous system and endocrine system of organisms. Animal experiments may show that exposure to this substance can cause behavioral abnormalities, reproductive disorders and other phenomena. Its migration and transformation in the environment expands the scope of influence, posing a potential threat to the integrity and stability of the ecological environment. In summary, this compound has a wide and complex impact in the environment, and it needs to be paid close attention and in-depth study to policy the safety of the ecological environment.

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