1 Diiodomethyl Sulfonyl 4 Methylbenzene
Iodobenzene

1 Diiodomethyl Sulfonyl 4 Methylbenzene

Fengxi Chemical

Specifications

HS Code

380558

Chemical Formula C8H8I2O2S
Molar Mass 409.92 g/mol
Appearance Solid (predicted, based on similar sulfonyl - containing aromatic compounds)
Melting Point No data found (but sulfonyl - aromatic compounds often have relatively high melting points due to strong intermolecular forces)
Boiling Point No data found (expected to be high considering the molecular weight and nature of the compound)
Solubility In Water Low (sulfonyl group can have some polar character, but the large hydrophobic benzene ring and iodine atoms dominate, making it insoluble in water)
Solubility In Organic Solvents Soluble in non - polar to moderately polar organic solvents like dichloromethane, chloroform, benzene (due to the non - polar benzene ring and the ability of the sulfonyl group to participate in some weak intermolecular interactions in organic media)
Density No data found (but expected to be relatively high due to the presence of heavy iodine atoms)
Vapor Pressure Low (high molecular weight and relatively strong intermolecular forces would result in low vapor pressure)
Stability Stable under normal conditions, but may be sensitive to strong reducing agents or extreme acidic/basic conditions which could disrupt the sulfonyl group or aromatic ring
Chemical Formula C8H8I2O2S
Molecular Weight 416.02
Appearance Solid (presumed, based on similar compounds)
Solubility In Water Low (due to non - polar benzene ring and hydrophobic groups)
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform (typical for organic sulfonyl compounds)
Vapor Pressure Low (due to its solid nature and relatively high molecular weight)
Name 1-[(diiodomethyl)sulfonyl]-4-methylbenzene
Chemical Formula C8H8I2O2S
Molar Mass 437.92 g/mol
Appearance Solid (predicted)
Melting Point Unknown
Boiling Point Unknown
Density Unknown
Solubility In Water Insoluble (predicted)
Solubility In Organic Solvents Soluble in common organic solvents (predicted)
Vapor Pressure Low (predicted)
Flash Point Unknown
Stability Stable under normal conditions (predicted)
Packing & Storage
Packing 100 - gram vial packaging for 1 - [(diiodomethyl)sulfonyl]-4 - methylbenzene chemical.
Storage 1 - [(Diiodomethyl)sulfonyl]-4 - methylbenzene should be stored in a cool, dry, well - ventilated area, away from sources of heat, ignition, and direct sunlight. Keep it in a tightly - sealed container to prevent exposure to air and moisture, which could potentially cause decomposition. Store it separately from incompatible substances like oxidizing agents and bases to avoid dangerous reactions.
Shipping 1 - [(diiodomethyl)sulfonyl]-4 - methylbenzene is a chemical. Shipping should comply with hazardous material regulations. It may need special packaging to prevent breakage and leakage during transit.
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1-[(diiodomethyl)sulfonyl]-4-methylbenzene 1-[(diiodomethyl)sulfonyl]-4-methylbenzene 1-[(diiodomethyl)sulfonyl]-4-methylbenzene
General Information
Frequently Asked Questions
What are the main uses of 1- [ (diiodomethyl) sulfonyl] -4-methylbenzene?
The (diterpene methyl) base is occasionally mentioned in the ancient alchemy cultivation and divine recipe. It is often used as a mysterious and strange object in the alchemy book, but it involves secrets and the whole picture.
As for its use, there are different methods in ancient practice books and monsters. First, in some alchemy schools of thought, the (diterpene methyl) base is rare and cited by the high-quality elixir. Because the ancients believed that this base has magical properties, it can be used in the process of alchemy, and the nature of alchemy, catalyzing the birth of alchemy, so that the alchemy has extraordinary effects, or can help people break through the practice bottle, or can prolong the life and health of the body.
Second, in some divine formulas, the (diterpene methyl) base is used in sacrificial prayers. According to the ancients, this material can communicate with the mind, sense the world, and be used as a sacrificial offering, or used to arrange special methods, which can increase the cost of sacrifice, pray for rain, eliminate misery, or use its nature to communicate with the mysterious power of heaven and earth, so as to achieve specific purposes.
And tetramethylsilicon, its main use is wide. In ancient gold and stone smelting, tetramethylsilicon can be used to improve the properties of gold. It is integrated into the metal smelting process in a certain proportion, which can make the metal more efficient, and the utensils are more sophisticated and durable. For example, in the first place, adding an amount of tetramethylsilicon can make the blade more efficient and not easy to fold, making it an important material for famous manufacturing.
In ancient construction fields, tetramethylsilicon is also used. It can be used in building materials to improve their waterproof and moisture-proof properties. With its brush on tiles and wood, it can form a protective film to prevent rain from invading and extend the life of the building. For example, in the construction of some ancient temples and temples, tetramethylsilicon is cleverly used to make the construction of buildings still stand tall.
What are the physical properties of 1- [ (diiodomethyl) sulfonyl] -4-methylbenzene

The color state of this substance, at room temperature, is mostly in the form of a solid state. Its texture is either fine powder or dense crystallization. Its appearance is often pure color, or white or nearly colorless, just like the purity of ice and snow and the purity of white jade.
When it comes to melting point, the melting point of (dicyanomethyl) and dinitro can quite show its characteristics. Due to the interaction and orderly arrangement of atoms in its molecular structure, its melting point is in a specific range. This specific melting point is a key physical quantity when identifying and separating this substance. It is like a precise ruler that helps chemists to distinguish its authenticity and separate its purity.
Its density cannot be ignored. Due to the mass and spatial arrangement of molecules, (dicyanomethyl) has a specific density with dinitro groups. This density data is indispensable for guiding the ratio of materials and process design in chemical production. It is like a nautical compass, leading the chemical process in the right direction.
In terms of solubility, this substance exhibits different solubility in specific solvents. In some organic solvents, such as alcohols and ethers, it may have a certain solubility; in polar solvents such as water, its solubility may be very low. This difference in solubility provides many possibilities and strategies for the separation, purification and construction of reaction systems, which is like a key to open the door to different chemical operations.
(dicyanomethyl) and the physical properties of dinitro groups, from color state to melting point, density and solubility, are like tightly interlocking rings, forming a unique picture of their physical properties, providing rich information and foundation for chemical research and application.
What are the chemical properties of 1- [ (diiodomethyl) sulfonyl] -4-methylbenzene
The chemical properties of (dibenzyl) thiazolinyl-4-methylbenzene are really important to explore. This compound has many unique chemical properties.
First of all, its structure contains thiazoline ring and benzyl group, which endows it with certain stability and special reactivity. The nitrogen and sulfur atoms in the thiazoline ring can participate in a variety of nucleophilic reactions due to their solitary pair electrons. For example, under appropriate conditions, it can undergo nucleophilic substitution reactions with electrophilic reagents. Nitrogen or sulfur atoms can be used as nucleophilic check points to attack electrophilic reagents and form new chemical bonds. This property may be used in organic synthesis to construct complex molecular structures.
Furthermore, the methylbenzene part, the benzene ring has a conjugated system, so that the compound has a certain electron delocalization characteristic. This causes it to have a specific response to external conditions such as light and heat. For example, under lighting conditions, the electron cloud distribution on the benzene ring changes or initiates photochemical reactions, or isomerization, or cycloaddition reactions, etc., providing the possibility for its application in the field of photochemistry.
In addition, the carbon-carbon bond in the benzyl group is connected to the benzene ring, and the electron cloud density on the benzyl carbon changes due to the electron-absorbing induction effect of the benzene ring. This makes benzyl group exhibit unique reactivity in some reactions, such as oxidation reactions or reactions with metal reagents. Benzyl carbon-hydrogen bonds may be oxidized under the action of a specific catalyst and converted into corresponding alcohols, aldons or carboxylic acids.
Moreover, the overall chemical properties of the compound are also affected by intermolecular interactions. Due to the existence of polar groups and non-polar parts in the molecule, its solubility and molecular aggregation state may vary in different solvents, which in turn affects its chemical behavior. In non-polar solvents, molecules may tend to aggregate through non-polar interactions, while in polar solvents, the interaction between polar groups and solvent molecules dominates, which affects the rate and selectivity of their participation in chemical reactions in solution.
What is the preparation method of 1- [ (diiodomethyl) sulfonyl] -4-methylbenzene?
The preparation of (dinitroethyl) nitrate and 4-ethyl nitrate requires a delicate recipe.
First of all, the preparation of (dinitroethyl) nitrate. Take suitable raw materials, such as compounds containing alcohol groups, and have an activity check point that can react with nitric acid groups. Place it in a clean container, which must be able to withstand reaction conditions, such as moderate temperature and pressure. With an appropriate amount of nitric acid as the nitrifying agent, the concentration of nitric acid should be precisely prepared. If it is too high, it will easily cause side reactions, and if it is too low, the reaction will be difficult to be sufficient. You can slowly drop nitric acid into the container containing the raw materials, and at the same time gently stir to mix the two evenly. The temperature of the reaction should be maintained within a specific range, which depends on the raw materials and reaction characteristics, or kept at a low temperature in an ice bath to prevent overreaction, or provided with moderate energy in a warm water bath to promote the reaction. In this process, the progress of the reaction must be monitored at all times, and the degree of reaction can be determined by chemical analysis methods, such as thin-layer chromatography. When the reaction reaches the expected level, the crude product of (dinitroethyl) nitrate is obtained. Subsequent steps of separation and purification, such as extraction, distillation, etc., are required to obtain a pure product.
As for the preparation of 4-ethyl nitrate, there is also a method. The reactant containing ethyl should be selected, and this reactant should have a suitable position where nitro can be introduced. Also in a suitable reaction vessel, add this reactant, followed by an appropriate nitrifying agent and catalyst. The choice of nitrifying agent is very critical, either a mixed acid of nitric acid and sulfuric acid, or other specific nitrifying reagents, depending on the characteristics of the reactants. The catalyst can also affect the rate and selectivity of the reaction, and needs to be selected with caution. During the reaction, control the temperature, pressure and reaction time. If the temperature is too high, the product may decompose or produce too many by-products; the regulation of pressure is related to the kinetic equilibrium of the reaction. After the reaction is completed, the product also needs to be carefully separated and purified to obtain pure 4-ethyl nitrate. Therefore, according to these methods, the required (dinitroethyl) nitrate and 4-ethyl nitrate can be obtained.
What are the precautions for 1- [ (diiodomethyl) sulfonyl] -4-methylbenzene during storage and transportation?
In the process of storage of dimethyl base powder-based and methyl base amine, it is necessary to pay more attention.
Dimethyl base powder-based ones have special properties, and they must be stored in a dry, dry, and good place. If the environment is wet, it is easy to cause the problem of deliquescence, which will cause it to be changed to the ground, and it will be used in the shadow of the day. And it needs to be stored separately. Because of its chemical activity, it is difficult for this material to be mixed with each other, and it is feared that it will become intense and react, and it will become dangerous. If it is too difficult, the package must be damaged to prevent leakage. It is also necessary to keep clear and dry, and avoid the mixing of other materials.
When it comes to methylamine, it is especially important to pay attention to low temperature in the environment. Because of its durability, if the temperature is slightly higher, it is easy to disperse, not only causing damage, but also irritating, endangering the health of people around the world. Storage also requires a source of ignition and fire, because it is flammable, in case of open fire or high temperature, it is flammable and explodes. On the way, in addition to the package being firm, it is necessary to keep the temperature, strength, etc. close. Once it is normal, immediately take the best policy to ensure safety.
In addition, both of these need to be stored according to their characteristics, and they need to abide by the rules and conditions, and operate carefully in order to prevent accidents, protect the safety of objects and make profits.