Tetrafluoro 2 Tetrafluoro 2 Iodoethoxy Ethanesulfonyl Fluoride
Iodobenzene

Tetrafluoro 2 Tetrafluoro 2 Iodoethoxy Ethanesulfonyl Fluoride

Fengxi Chemical

Specifications

HS Code

457734

Chemical Formula C4F10O3SIF
Molecular Weight 442.00
Appearance Typically a colorless to pale - yellow liquid
Boiling Point Specific value depends on pressure conditions, generally in a certain range for such fluorinated sulfonyl compounds
Melting Point Data may vary, characteristic for this type of organic fluorine compound
Density Appropriate value for a compound of this structure and composition
Solubility Solubility characteristics in common organic solvents like hydrocarbons, ethers, etc.
Vapor Pressure A certain value related to its volatility at given temperatures
Stability Stable under normal storage conditions, but may react under specific chemical environments
Reactivity Can participate in reactions typical for sulfonyl fluoride and iodo - containing fluorinated ethers
Chemical Formula C4F9IO3S
Molecular Weight 426.001
Chemical Formula C4F9IO3S
Molar Mass 406.00 g/mol
Chemical Formula C4F10O2SIF
Molecular Weight 422.002
Packing & Storage
Packing 100g of Tetrafluoro - 2-(tetrafluoro - 2 - iodoethoxy)ethanesulfonyl Fluoride in sealed container.
Storage Tetrafluoro - 2-(tetrafluoro - 2 - iodoethoxy)ethanesulfonyl Fluoride should be stored in a cool, dry, well - ventilated area. Keep it away from heat sources, ignition sources, and incompatible substances. Store in a tightly - sealed container to prevent leakage. Given its chemical nature, store it in a location separate from reactive chemicals to avoid potential reactions.
Shipping Tetrafluoro - 2 - (tetrafluoro - 2 - iodoethoxy)ethanesulfonyl Fluoride is a chemical. Shipping requires proper containment in specialized vessels, following strict regulations for hazardous chemicals to ensure safety during transit.
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Tetrafluoro-2-(tetrafluoro-2-iodoethoxy)ethanesulfonyl Fluoride Tetrafluoro-2-(tetrafluoro-2-iodoethoxy)ethanesulfonyl Fluoride Tetrafluoro-2-(tetrafluoro-2-iodoethoxy)ethanesulfonyl Fluoride
General Information
Frequently Asked Questions
What are the main uses of Tetrafluoro-2- (tetrafluoro-2-iodoethoxy) ethanesulfonyl Fluoride?
Tetrafluoro-2- (tetrafluoro-2-iodoethoxy) ethanesulfonyl fluoride has a wide range of uses. In the field of organic synthesis, it is often used as a key reagent. Due to its unique structure, fluorine-containing groups give special properties, which can introduce target molecules and greatly change the physical and chemical properties of compounds, such as improving stability and enhancing fat solubility. It is of great significance in the creation of novel organic materials and drug development.
In the field of materials science, high-performance fluoropolymers can be prepared using this substance. By connecting it to the main chain or side chain of the polymer through a specific reaction, the polymer has excellent chemical resistance, low friction coefficient and excellent thermal stability, and is widely used in aerospace, electronics industry and other fields that require strict material properties.
In the field of pharmaceutical chemistry, it may participate in the construction of new drug molecules. By virtue of the fluorine-containing structure, it affects the biological activity, metabolic stability and membrane permeability of drug molecules, helping to develop innovative drugs with good efficacy and small side effects. At the same time, in some special reactions, it can also act as a fluorination reagent or sulfonylation reagent, promoting the efficient progress of organic synthesis reactions, providing an effective way for the synthesis of complex organic compounds, and playing an important role in the development process of organic synthesis chemistry.
What are the physical properties of Tetrafluoro-2- (tetrafluoro-2-iodoethoxy) ethanesulfonyl Fluoride
Tetrafluoro-2- (tetrafluoro-2-iodoethoxy) ethanesulfonyl fluoride, this substance is an organic compound with unique physical properties.
Looking at its properties, it may be a colorless to slightly yellow liquid under normal conditions. Due to the characteristics of fluorine, iodine and other elements in the molecular structure, it appears like this. Its boiling point and melting point are also determined by the intermolecular forces and structures. Due to the high electronegativity of fluorine atoms in the molecule, there is a strong van der Waals force between molecules, so the boiling point may be relatively high, but the exact value needs to be determined experimentally and accurately.
When it comes to solubility, given that it contains sulfonyl fluoride groups and has a certain polarity, it may have good solubility in polar organic solvents such as acetone and acetonitrile, and can be mutually soluble with solvent molecules through dipole-dipole interaction; in non-polar solvents such as n-hexane, the solubility may be poor, due to the mismatch between molecular polarity and non-polar solvents.
Furthermore, its density varies depending on the type and quantity of atoms in the molecule. Fluorine and iodine atoms are relatively large in atomic weight, resulting in an increase in molecular weight. In addition, the molecules are closely arranged, and their density may be greater than that of common organic solvents, or in the range of 1.5-2.5 g/cm ³, but the actual measurement needs to be experimentally measured.
In addition, the compound is volatile or low, and due to the strong intermolecular force, it requires high energy for molecules to break away from the liquid surface and enter the gas phase. This property makes it relatively stable at room temperature and pressure, and it is not prone to volatilization loss.
What are the chemical properties of Tetrafluoro-2- (tetrafluoro-2-iodoethoxy) ethanesulfonyl Fluoride
Tetrafluoro-2- (tetrafluoro-2-iodoethoxy) ethanesulfonyl fluoride has specific chemical properties. It is active and shows a unique state in many reactions.
Looking at its structure, it contains many fluorine atoms. Fluoride is also an element with strong electronegativity, resulting in high stability of the compound and very low surface energy. In this way, it may have the characteristics of water and oil repellent, and can be used to create special materials, such as waterproof fabrics, anti-fouling coatings, etc.
The presence of iodine atoms also adds chemical activity. Iodine atoms can participate in various substitution reactions, introducing new ways for organic synthesis. Under appropriate conditions, iodine atoms can be replaced by other functional groups to build complex organic molecular structures.
Furthermore, sulfonyl fluoride groups endow compounds with acidic properties. Sulfonyl fluoride can be hydrolyzed, releasing protons in specific environments, and may play a role in catalytic reactions or some ion exchange processes.
Because of its special groups such as fluoride, iodine and sulfonyl fluoride, tetrafluoro-2- (tetrafluoro-2-iodoethoxy) ethanesulfonyl fluoride has broad application prospects in organic synthesis, materials science and other fields. It can be used as a starting material for the creation of new functional materials and can also be a key reagent for the development of organic reactions.
What is the synthesis method of Tetrafluoro-2- (tetrafluoro-2-iodoethoxy) ethanesulfonyl Fluoride
To prepare Tetrafluoro - 2 - (tetrafluoro - 2 - iodoethoxy) ethanesulfonyl Fluoride, the following ancient method can be used.
First, choose a suitable starting material, based on fluorine-containing compounds, such as specific fluorinated alcohols or fluorinated halogenated hydrocarbons. Take fluorinated alcohols, such as 2,2,3,3 - tetrafluoropropanol, and halogenating agents, such as phosphorus trichloride or phosphorus pentachloride, in appropriate proportions, in a reaction kettle at a suitable temperature, under the protection of an inert gas such as nitrogen. This step aims to convert the alcohol hydroxyl group into halogen atoms to form halogens.
Then, take the prepared halogen and reflux it with an iodide reagent, such as sodium iodide or potassium iodide, in a polar solvent, such as acetone. After nucleophilic substitution, the halogen atom is replaced by an iodine atom to obtain an iodine intermediate.
Then the iodine intermediate is reacted with a sulfonyl fluoride-containing reagent, such as fluorosulfonic anhydride, in the presence of a base, such as potassium carbonate, in an organic solvent, such as dichloromethane, at low temperature. The function of the base is to promote the reaction, grab protons, and move the reaction in the direction of generating the target product.
After the reaction is completed, the unreacted raw materials and by-products are removed by conventional separation and purification methods, such as distillation, column chromatography, etc., to obtain pure Tetrafluoro-2 - (tetrafluoro-2 - iodoethoxy) ethanesulfonyl Fluoride. During this period, the operation must be careful to prevent the toxicity and corrosiveness of fluoride, and pay attention to the control of reaction conditions to increase the yield and purity of the product.
What are the precautions for the use of Tetrafluoro-2- (tetrafluoro-2-iodoethoxy) ethanesulfonyl Fluoride
Tetrafluoro-2- (tetrafluoro-2-iodoethoxy) ethanesulfonyl fluoride is a chemical agent. During use, many matters need to be paid attention to.
The first is about safety protection. Because of its chemical activity, or potential harm to the human body. When operating, it is necessary to wear appropriate protective equipment, such as laboratory clothes, gloves, goggles, etc., to avoid contact with the skin and eyes. If this substance accidentally touches the skin, it should be rinsed with plenty of water immediately. If you feel unwell, seek medical treatment immediately; if it enters the eyes, rinse with plenty of water immediately and seek medical attention as soon as possible.
Furthermore, it is related to the operating environment. It should be used in a well-ventilated place to prevent the accumulation of harmful gases. If operated in a confined space, the gas concentration is too high, or it may cause respiratory irritation or even poisoning. Ventilation equipment can effectively discharge volatile gases to ensure the safety of operators.
Storage should also not be ignored. It should be placed in a cool, dry and ventilated place, away from fire and heat sources. Due to its chemical properties, there may be a risk of combustion and explosion under high temperature or open flame environment. At the same time, it should be placed separately from other chemicals to avoid mutual reaction.
The dosage and method of use must be precisely controlled. It should be used strictly according to the experimental or production requirements. Improper dosage or uncontrolled reaction may affect the experimental results or production quality, and may also cause safety accidents.
Use appropriate appliances during access to avoid leakage or contamination with other substances due to improper appliances. After operation, properly dispose of remaining substances and waste, follow relevant environmental regulations, and do not discard them at will to avoid polluting the environment.