3 Iodobenzotrifluoride
Iodobenzene

3 Iodobenzotrifluoride

Fengxi Chemical

Specifications

HS Code

619408

Chemical Formula C7H4F3I
Molecular Weight 286.009
Appearance Colorless to light yellow liquid
Boiling Point 188 - 190 °C
Density 1.914 g/mL at 25 °C
Solubility Insoluble in water, soluble in organic solvents
Flash Point 77 °C
Refractive Index 1.525 - 1.527
Chemical Formula C7H4F3I
Molecular Weight 286.009
Appearance Colorless to light yellow liquid
Boiling Point 187 - 188 °C
Density 1.858 g/mL at 25 °C
Solubility Insoluble in water, soluble in organic solvents like ethanol, ether
Flash Point 74.4 °C
Refractive Index 1.5300 - 1.5320
Chemical Formula C7H4F3I
Molecular Weight 286.009
Appearance Colorless to light yellow liquid
Boiling Point 197 - 198 °C
Density 1.939 g/mL at 25 °C
Flash Point 75.6 °C
Solubility Insoluble in water, soluble in organic solvents
Refractive Index 1.522 - 1.524
Chemical Formula C7H4F3I
Molecular Weight 272.009
Appearance Colorless to light yellow liquid
Boiling Point 196 - 198 °C
Melting Point N/A
Density 1.855 g/mL at 25 °C
Vapor Pressure N/A
Solubility Insoluble in water, soluble in organic solvents like ethanol, ether
Flash Point 76.7 °C
Refractive Index 1.527 - 1.529
Packing & Storage
Packing 100 - gram bottle of 3 - iodobenzotrifluoride, tightly sealed for chemical safety.
Storage 3 - iodobenzotrifluoride should be stored in a cool, dry, well - ventilated area. Keep it away from heat sources, open flames, and oxidizing agents. Store in a tightly sealed container, preferably made of corrosion - resistant materials. This helps prevent leakage and degradation, ensuring its stability and minimizing the risk of hazardous reactions.
Shipping 3 - iodobenzotrifluoride is a chemical. Ship it in proper, leak - proof containers, following all regulations for hazardous chemicals. Ensure proper labeling and documentation during transportation to guarantee safety.
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3-iodobenzotrifluoride 3-iodobenzotrifluoride 3-iodobenzotrifluoride
General Information
Frequently Asked Questions
What is the chemistry of 3-iodobenzotrifluoride?
3-Iodine trifluorotoluene has specific chemical properties and is worth studying. Among this substance, the iodine atom is active and easy to involve the reaction of nucleophilic substitution. The cover iodine atom has a large radius and the C-I bond energy is weak. Under appropriate reagents and conditions, iodine is easy to be replaced by other groups. In case of nucleophilic reagents, such as alkoxides, amines, etc., iodine can be replaced by corresponding groups to form new organic compounds. This is widely used in organic synthesis.
and its trifluoromethyl group have strong electronegativity and can cause a significant increase in molecular polarity. This property affects its physical properties, such as boiling point, solubility, etc., and in terms of reactivity, the density of adjacent and para-electron clouds decreases, the electrophilic substitution activity of aromatic rings changes, and multiple meta-substitution products are formed.
Its stability is also an important property. Although iodine is more active, the existence of trifluoromethyl groups stabilizes its structure to a certain extent. Under normal conditions, its chemical properties can be relatively stable. However, under extreme conditions such as strong oxidizing agents, reducing agents or high temperatures, the structure can still change, triggering a variety of chemical reactions.
Furthermore, it can be used as a key intermediate in organic synthesis. Through the substitution of iodine and the unique effect of trifluoromethyl, multiple and complex organic molecular structures can be constructed, providing an important cornerstone for the creation of new medicines, pesticides and functional materials. In short, 3-iodine trifluorotoluene occupies an important place in the field of organic chemistry due to its uniqueness.
What are the common uses of 3-iodobenzotrifluoride?
3-Iodotrifluorotoluene has the following common uses.
First, it is often used as a key intermediate in the field of organic synthesis. Due to its special structure, iodine atoms have good activity and can participate in many classical reactions, such as the Suzuki reaction. In this reaction, 3-iodotrifluorotoluene and boron-containing compounds can be formed under the action of specific catalysts. Carbon-carbon bonds can be formed, and then a series of organic molecules with special structures and functions can be synthesized, such as complex pharmaceutical intermediates or functional material precursors. For example, in the Ullmann reaction, it can react with phenols and other compounds to form aromatic ethers with specific substituents, which are important in flavors, pesticides and other fields.
Second, it also has uses in materials science. Because it contains trifluoromethyl, it imparts unique physical and chemical properties to the molecule, such as excellent thermal stability, chemical stability and low surface energy. Polymer materials synthesized from this raw material may have special electrical and optical properties, and can be used in liquid crystal materials, semiconductor materials and other fields to improve the performance and application range of materials.
Third, in the field of pharmaceutical research and development, 3-iodotrifluorotoluene is used as a starting material, and a molecular structure with biological activity can be constructed through multi-step reaction. Due to its special chemical structure, the introduction of drug molecules may change the lipophilicity, metabolic stability and other properties of the compound, which helps to improve the bioavailability and efficacy of the drug, so it plays an important role in the process of creating new drugs.
Fourth, in the field of pesticide chemistry, pesticides synthesized on this basis, or due to the existence of trifluoromethyl and iodine atoms, exhibit efficient killing or inhibitory activity on specific pests or weeds, and with its stability, it can maintain a certain drug effect in the environment, providing an effective means for agricultural pest control.
What are 3-iodobenzotrifluoride synthesis methods?
There are several common methods for the synthesis of 3-iodotrifluorotoluene.
One is to use 3-aminotrifluorotoluene as the starting material and obtain it by diazotization and iodine substitution. First, 3-aminotrifluorotoluene is diazotized with sodium nitrite in an acidic medium to form a diazonium salt. This reaction requires strict temperature control, usually at low temperature to prevent the decomposition of diazonium salts. Then, the resulting diazonium salt is reacted with iodine sources such as potassium iodide, and the diazonium group is replaced by iodine atoms to obtain 3-iodotrifluorotoluene. The advantage of this method is that the reaction steps are relatively clear and the yield is acceptable; however, there are also disadvantages, such as the price of raw material 3-amino trifluorotoluene or higher, and the diazotization reaction operation needs to be cautious and the reaction conditions are strict.
The second can be prepared from 3-halogenated trifluorotoluene (such as 3-chlorotrifluorotoluene or 3-bromotrifluorotoluene) by halogen exchange reaction. Taking 3-chlorotrifluorotoluene as an example, under appropriate catalyst and reaction conditions, it reacts with iodizing reagents (such as sodium iodide, etc.), and the chlorine atom is replaced by the iodine atom. This reaction requires the selection of suitable catalysts to promote the smooth progress of the reaction, such as some transition metal catalysts. The raw materials of this method are relatively easy to obtain. However, the halogen exchange reaction or the presence of incomplete reaction conditions affects the purity and yield of the product, and the choice and amount of catalyst have a great influence on the reaction result.
Third, benzene is used as the starting material and synthesized through a multi-step reaction. First, the trifluoromethylation of benzene is carried out, the trifluoromethyl is introduced, and then the halogenation reaction is carried out at a specific position, the halogen atom is introduced, and finally the halogen atom is converted into an iodine atom by halogen atom exchange or other suitable methods. This route has many steps and complex reaction conditions, and the reaction conditions of each step need to be precisely controlled to ensure the selectivity and yield of the product. However, its advantage is that the starting material benzene is widely sourced and inexpensive. If the reaction conditions
The methods for synthesizing 3-iodotrifluorotoluene have their own advantages and disadvantages. In practical application, the appropriate synthesis route should be selected according to specific needs, such as raw material cost, product purity, production scale and other factors.
3-iodobenzotrifluoride need to pay attention to when storing and transporting
3-Iodotrifluorotoluene is an organic compound. When storing and transporting, many key matters must be paid attention to.
First words storage. This substance should be stored in a cool, dry and well-ventilated place. Because of its certain chemical activity, high temperature and humid environment are prone to qualitative change. Warehouse temperature should be controlled within a specific range to prevent excessive temperature from causing its volatilization to intensify, or triggering chemical reactions. And it should be kept away from fires and heat sources. Because it may be flammable, open flames and hot topics may cause danger, such as fires or even explosions.
Furthermore, storage should be separated from oxidants, reducing agents, alkalis, etc., and must not be mixed. This is because 3-iodotrifluorotoluene may react violently with the above substances, which will damage the purity of the substance and even endanger safety. At the same time, the warehouse needs to be equipped with suitable materials to contain the leakage, so as to prevent the accidental leakage from being properly handled in time and reduce the harm.
Second talk about transportation. Before transportation, ensure that the packaging is complete and well sealed. The packaging material needs to be able to resist vibration, collision and environmental factors to prevent the leakage of substances caused by the damage of the container during transportation. The transportation process should also be kept away from fire and heat sources. The transportation vehicle should be equipped with the corresponding variety and quantity of fire-fighting equipment and leakage emergency treatment equipment.
In addition, the transportation should be carried according to the specified route, and do not stop in densely populated areas, residential areas, etc. If the transportation vehicle encounters a malfunction or other accident, it needs to be dealt with in accordance with the emergency plan in a timely manner and promptly reported to the relevant departments. The escort personnel should also be familiar with the characteristics of the transported substances and emergency treatment methods, and carefully guard the whole process to ensure the safety of transportation. In this way, when storing and transporting 3-iodotrifluorotoluene, avoid disasters and ensure the safety of its quality, environment and personnel.
3-iodobenzotrifluoride impact on the environment and human health
3-Iodotrifluorotoluene, an organic compound, is widely used in many industrial fields such as medicine, pesticides and material synthesis. However, it has potential effects on the environment and human health.
At the environmental level, 3-iodotrifluorotoluene has a certain persistence and is difficult to degrade rapidly in the natural environment. Once released into the environment, it can be retained in soil, water and atmosphere for a long time. In soil, it may affect the community structure and function of soil microorganisms, hindering the material cycle and energy conversion of soil ecosystems. After entering the water body, it will cause toxicity to aquatic organisms. Because it is fat-soluble, it is easy to accumulate in aquatic organisms and is transmitted through the food chain, harming higher nutrient-level organisms. In the atmosphere, or participate in photochemical reactions, affect atmospheric quality, and have indirect effects on regional and even global climate.
As far as human health is concerned, 3-iodine trifluorotoluene can enter the human body through inhalation, skin contact and accidental ingestion. Inhalation of air containing this substance may irritate the respiratory tract, causing symptoms such as cough, asthma, and breathing difficulties. Long-term exposure may damage lung function and increase the chance of respiratory diseases. Skin contact may cause skin allergies, redness, swelling, itching and other reactions. If accidentally ingested, it will irritate the gastrointestinal tract, causing nausea, vomiting, abdominal pain, etc. And animal experiments have shown that the substance may have certain genetic toxicity and carcinogenicity, long-term exposure, or increase the risk of cancer in the human body.
In summary, when using 3-iodotrifluorotoluene, it is necessary to take proper protective measures and strengthen environmental monitoring to reduce its potential harm to the environment and human health.