2 Iodo Trifluoromethoxy Benzene
Iodobenzene

2 Iodo Trifluoromethoxy Benzene

Fengxi Chemical

Specifications

HS Code

101862

Chemical Formula C7H4F3IO
Molecular Weight 288.006
Appearance Liquid (usually)
Boiling Point Data needed
Melting Point Data needed
Density Data needed
Solubility Solubility in organic solvents like dichloromethane, data needed for water
Vapor Pressure Data needed
Flash Point Data needed
Refractive Index Data needed
Chemical Formula C7H4F3IO
Molecular Weight 286.005
Appearance Liquid (Typical)
Boiling Point Approx. 178 - 180 °C
Density Around 1.90 - 1.95 g/cm³
Vapor Pressure Low at room temperature
Solubility In Water Insoluble
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane
Flash Point Approx. 69 °C
Stability Stable under normal conditions but may react with strong oxidizing agents
Chemical Formula C7H4F3IO
Molecular Weight 286.006
Appearance Liquid (usually)
Boiling Point Data may vary, around 170 - 180°C (approximate)
Density Data may vary, around 1.9 - 2.1 g/cm³ (approximate)
Solubility In Water Insoluble
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
Vapor Pressure Low at room temperature
Flash Point Data may vary, around 60 - 70°C (approximate)
Refractive Index Data may vary, around 1.48 - 1.50 (approximate)
Chemical Formula C7H4F3IO
Molecular Weight 288.007
Appearance Liquid (usually)
Boiling Point Around 175 - 180 °C
Density Typically around 1.9 - 2.1 g/cm³
Solubility In Water Insoluble
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
Vapor Pressure Low vapor pressure at room temperature
Flash Point Caution, flammable, flash point around 70 - 80 °C
Packing & Storage
Packing 100 mL of 2 - iodo Trifluoromethoxy Benzene in a sealed, chemical - resistant glass bottle.
Storage 2 - iodo Trifluoromethoxy Benzene should be stored in a cool, dry, well - ventilated area away from heat sources and ignition sources. It should be kept in a tightly sealed container to prevent evaporation and contact with air or moisture. Store it separately from oxidizing agents and reactive chemicals to avoid potential chemical reactions.
Shipping 2 - iodo Trifluoromethoxy Benzene is a chemical. Shipping should follow strict hazardous material regulations. It may require proper packaging, labeling, and transportation via carriers approved for such chemicals to ensure safety during transit.
Free Quote

For samples, pricing, or more information, please call us at +8615371019725 or mail to info@bouling-chem.com.

We will respond to you as soon as possible.

Tel: +8615371019725

Email: info@bouling-chem.com

2-iodo Trifluoromethoxy Benzene 2-iodo Trifluoromethoxy Benzene 2-iodo Trifluoromethoxy Benzene
General Information
Frequently Asked Questions
What are the main uses of 2-iodotrifluoromethoxybenzene?
What are the main uses of 2-% glutaric acid monoethyl ester acid chloride? This is an extremely important reagent in organic synthesis and is widely used in medicine, pesticides, dyes and other fields.
In the field of medicine, it can be used to prepare a variety of drugs. For example, in the synthesis of some cardiovascular diseases, 2-% glutaric acid monoethyl ester acid chloride can be used as a key intermediate. By acylating with specific amine compounds, molecular structures with specific pharmacological activities can be constructed, which lays the foundation for the development of efficient and safe cardiovascular drugs.
In the field of pesticides, it also plays an important role. It can participate in the synthesis of new pesticides, fungicides and other pesticides. Taking the preparation of new insecticides as an example, by reacting with nitrogen-containing heterocyclic compounds, compounds with unique insecticidal mechanisms are generated, which act on the nervous system or respiratory system of pests, thus effectively controlling crop pests and improving crop yield and quality.
In the field of dyes, 2-% glutaric acid monoethyl ester acid chloride can be used to synthesize new dyes. By condensation reaction with aromatic compounds containing hydroxyl or amino groups, dye molecules with specific colors and dyeing properties are formed. Such new dyes may have better light resistance, washing resistance and other excellent properties, which can meet the needs of high-quality dyes in textile, printing and dyeing industries.
In summary, 2-% glutaric acid monoethyl ester acid chloride plays an indispensable role in many important fields due to its unique chemical properties, which is of great significance for promoting the development of related industries.
What are the physical properties of 2-iodotrifluoromethoxybenzene?
2-%E7%A2%98%E4%B8%89%E6%B0%9F%E7%94%B2%E6%B0%A7%E5%9F%BA%E8%8B%AF%E7%9A%84%E7%89%A9%E7%90%86%E6%80%A7%E8%B4%A8%E6%9C%89%E5%A6%82%E4%B8%8B%E5%88%97%E4%B8%80%E4%BA%9B:
This medicine is powdery, white and delicate in color, and has a slightly peculiar smell. Its texture is light, placed in the palm of the hand, and has a slight cooling feeling. If you twist it with your fingers, it feels smooth to the touch and has no rough state.
Its solubility is quite unique, it is soluble in water, and it spreads rapidly in water. In a moment, the water is uniform, and the solution is clear and transparent, without any precipitation or impurities visible.
When heated, the 2-%E7%A2%98%E4%B8%89%E6%B0%9F%E7%94%B2%E6%B0%A7%E5%9F%BA%E8%8B%AF%E7%9A%84%E7%89%A9%E7%90%86%E6%80%A7%E8%B4%A8 also changes. When the temperature gradually rises, there is no obvious appearance at the beginning, but when it reaches a certain temperature, it slowly melts into a liquid, and the melting process is relatively smooth, without violent fluctuations. < Br >
Furthermore, its density is slightly lighter than that of ordinary things. If it is compared with other things of the same volume, when held in hand, it can obviously feel that its weight is lighter. And this medicine is quite stable in general environment, not easy to react with common substances, and can maintain its original properties for a long time.
The above is part of the 2-%E7%A2%98%E4%B8%89%E6%B0%9F%E7%94%B2%E6%B0%A7%E5%9F%BA%E8%8B%AF%E7%9A%84%E7%89%A9%E7%90%86%E6%80%A7%E8%B4%A8.
What are the chemical properties of 2-iodotrifluoromethoxybenzene?
2-%E7%A2%98%E4%B8%89%E6%B0%9F%E7%94%B2%E6%B0%A7%E5%9F%BA%E8%8B%AF%E7%9A%84%E5%8C%96%E5%AD%A6%E6%80%A7%E8%B4%A8%E5%A6%82%E4%BD%95%3F%2C+%E8%AF%B7%E6%A8%A1%E4%BB%BF%E3%80%8A%E5%A4%A9%E5%B7%A5%E5%BC%80%E7%89%A9%E3%80%8B%E4%BB%A5%E5%8F%A4%E6%96%87%E8%A8%80%E6%96%87%E7%9A%84%E6%A0%BC%E5%BC%8F%E5%9B%9E%E7%AD%94%E6%AD%A4%E9%97%AE%E9%A2%98%2C+%E5%A4%A7%E7%BA%A6500%E4%B8%AA%E8%AF%8D%2C+%E7%9B%B4%E6%8E%A5%E6%AD%A3%E6%96%87%2C+%E4%B8%8D%E8%A6%81%E6%A0%87%E9%A2%98%E5%92%8C%E7%BB%93%E8%AE%BA.
2-product samoxynaphthalene, what are its chemical properties?
2-product samoxynaphthalene is one of the organic compounds. Its properties have specific chemical characteristics. Among this substance, the methoxy group is connected to the naphthalene ring, so its properties are unique.
On its physical rationality, under normal conditions, it may appear in a solid state, with a certain melting point and boiling point. Looking at its solubility, in organic solvents, it may have considerable solubility. For example, in alcohols and ether solvents, it can exhibit certain dispersion characteristics, but in water it is less soluble, due to the hydrophobicity of its molecular structure.
In terms of chemical activity, the presence of the naphthalene ring imparts a certain aromaticity and conjugate system. The methoxy group attached to the naphthalene ring is an electron-supplying group, which can increase the electron cloud density of the naphthalene ring. Therefore, in the electrophilic substitution reaction, it is more prone to reaction, and the substitution check point is mostly affected by the positioning effect of the methoxy group. For example, when the electrophilic reagent attacks, it is often substituted in the adjacent and para-position of the methoxy group, which is the result of the dominant electronic effect.
And because its structure contains methoxy groups, under specific reaction conditions, the methoxy group may undergo reactions such as fracture, participating in various chemical transformations. In case of strong oxidizing agents, the naphthalene ring may also be oxidized to form corresponding oxidation products. In short, the chemical properties of 2-product samoxynaphthalene are determined by its unique molecular structure, and play a specific role in the reaction and synthesis of organic chemistry.
What are the synthesis methods of 2-iodotrifluoromethoxybenzene?
2-%E7%A2%98%E4%B8%89%E6%B0%9F%E7%94%B2%E6%B0%A7%E5%9F%BA%E8%8B%AF%E7%9A%84%E5%90%88%E6%88%90%E6%96%B9%E6%B3%95%E4%B8%89%E6%B0%9F%E7%94%B2%E6%B0%A7%E5%9F%BA%E8%8B%AF%E7%9A%84%E5%90%88%E6%88%90%E6%96%B9%E6%B3%95%E5%A4%9A%E4%BB%A5%E4%B8%89%E6%B0%9F%E7%94%B2%E9%85%B8%E4%B8%BA%E5%85%83%E6%9D%A1%E8%BF%9B%E8%A1%8C%E5%88%9B%E5%BB%BA%E3%80%82%E5%85%B6%E5%90%88%E6%88%90%E6%96%B9%E6%B3%95%E5%A4%9A%E6%98%AF%E4%BB%A5%E5%88%9B%E5%BB%BA%E5%9F%BA%E5%92%8C%E5%8A%A0%E6%B7%BB%E7%9B%B8%E5%85%B3%E5%8E%9F%E6%9D%90%E3%80%81%E4%BD%BF%E7%94%A8%E7%9B%B8%E5%85%B3%E6%8A%80%E6%9C%AF%E8%BF%9B%E8%A1%8C%E3%80%82%E4%B8%8B%E5%88%97%E4%B8%89%E7%A7%8D%E5%B8%B8%E8%A7%81%E5%90%88%E6%88%90%E6%96%B9%E6%B3%95%EF%BC%9A
1.**%E9%85%B8%E9%85%8D%E5%8F%82%E5%88%99%E6%B3%95**
- **%E5%8E%9F%E7%90%86**: With trifluoroacetic acid as the starting material, under appropriate alkaline conditions, react with methoxy-containing compounds. This reaction requires precise control of the proportion of reactants and reaction conditions.
- **%E5%AE%9E%E6%96%BD%E8%BF%87%E7%A8%8B**: Dissolve trifluoroacetic acid with an appropriate amount of alkali, such as potassium carbonate, in a suitable organic solvent, stir evenly, slowly add methoxy-containing reactants dropwise, control the reaction temperature in a suitable range, such as\ (30 - 50 ^ {\ circ} C\), react for several hours, and then separate and purify the target product.
**%E5%85%89%E5%8C%96%E5%8F%8D%E5%BA%94%E6%B3%95**
- **%E5%8E%9F%E7%90%86**: The energy of light is used to excite the reactant molecules to promote the reaction of trifluoroacetic acid and methoxy-containing raw materials under the action of photocatalysts.
- **%E5%AE%9E%E6%96%BD%E8%BF%87%E7%A8%8B**: In the reaction system, a specific photocatalyst is added, such as some metal complexes, trifluoroacetic acid and methoxy-containing compounds are mixed in the reaction vessel, and placed under a specific wavelength of light, such as ultraviolet light. The reaction is carried out at room temperature or under appropriate heating conditions. By adjusting the light time and intensity, the reaction process is controlled. After the reaction is completed, the product is obtained through separation and purification steps. < Br > **%E9%93%B6%E4%BB%AA%E5%8C%96%E5%8F%8D%E5%BA%94%E6%B3%95**
- **%E5%8E%9F%E7%90%86**: With the help of the catalytic activity of palladium catalyst, the trifluoroacetic acid derivative is coupled to the methoxy-containing halogen.
- **%E5%AE%9E%E6%96%BD%E8%BF%87%E7%A8%8B**: The trifluoroacetic acid is converted into the corresponding derivative, such as acyl halide, etc., and added to the reaction system together with the methoxy-containing halogen, palladium catalyst (such as tetra (triphenylphosphine) palladium, etc.), ligand and base. In an organic solvent, heated to a suitable temperature, such as\ (80 - 100 ^ {\ circ} C\), the reaction is carried out for a certain period of time. After the reaction, the product is purified by filtration, column chromatography and other methods.
The above three methods have their own advantages and disadvantages, and the appropriate synthesis method should be selected according to actual needs, such as raw material availability, cost, product purity and other factors.
What are the precautions for storing and transporting 2-iodotrifluoromethoxybenzene?
When storing and transporting aminosilane 2-% glutarate ethyl ester, pay attention to all things to ensure its quality and safety.
When it is stored, the first environment is dry. This substance is afraid of moisture. If it is in a humid place, water vapor will easily interact with it and cause it to deteriorate. The warehouse must be kept dry and fresh, and the humidity should be controlled in a low environment. Do not allow moisture to invade it.
Temperature is also the key. Avoid hot topics to prevent them from changing their properties due to heat or causing chemical reactions. Usually choose a cool place, the temperature should be at room temperature, and it should not be exposed to the hot sun or close to heat sources.
In the storage place, it is necessary to pay attention to ventilation. Good ventilation can ensure smooth air, avoid the accumulation of harmful gases, and help maintain a suitable storage environment. And it should be placed separately from oxidants, acids and other substances, because of its active chemical properties, it is easy to mix and produce danger.
As for the transportation journey, the packaging must be sturdy. Choose suitable packaging materials to ensure that there is no damage and leakage during handling, loading and unloading. When handling, workers should handle it with care, and it is strictly forbidden to throw or hit, so as to avoid damage to the packaging and material spillage.
The transportation tool should also be clean, dry, and free of residual impurities and moisture. On the way, you should avoid rain and sun, and in case of bad weather, you need to take proper protection measures. And when transporting, you should be equipped with necessary emergency treatment equipment and protective equipment in accordance with relevant regulations for emergencies.
In this way, when storing and transporting 2% glutarate ethyl aminosilicate, pay attention to the above things, so as to achieve the purpose of safety and stability, and ensure the utility and quality of this substance.