2 Bromo 5 Iodo 1 3 Dimethylbenzene
Iodobenzene

2 Bromo 5 Iodo 1 3 Dimethylbenzene

Fengxi Chemical

Specifications

HS Code

434691

Chemical Formula C8H8BrI
Molar Mass 311.96 g/mol
Appearance Solid (predicted, actual appearance may vary)
Physical State At Room Temperature Solid
Boiling Point Estimated high due to large and heavy substituents
Solubility In Water Low, non - polar nature
Solubility In Organic Solvents Soluble in non - polar organic solvents like hexane, benzene
Vapor Pressure Low due to its solid state and relatively large molecular mass
Name 2-bromo-5-iodo-1,3-dimethylbenzene
Molecular Formula C8H8BrI
Molecular Weight 309.96
Appearance Typically a liquid or solid (description may vary by purity and conditions)
Physical State At Room Temperature Likely liquid
Boiling Point Data depends on purity, but generally higher due to large halogen atoms
Melting Point Specific value depends on purity and structure details
Density Data varies based on purity and temperature
Solubility In Water Low solubility, as it is non - polar due to the benzene ring and non - polar substituents
Solubility In Organic Solvents Soluble in common organic solvents like chloroform, dichloromethane
Flash Point Data needed from experimental determination
Stability Stable under normal conditions, but may react with strong oxidizing agents
Chemical Formula C8H8BrI
Molar Mass 309.96 g/mol
Appearance Solid (likely colorless to pale yellow)
Melting Point Data needed
Boiling Point Data needed
Density Data needed
Solubility In Water Insoluble
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, acetone
Odor Characteristic aromatic odor
Stability Stable under normal conditions
Name 2-bromo-5-iodo-1,3-dimethylbenzene
Molecular Formula C8H8BrI
Molecular Weight 309.96
Appearance Solid (likely)
Boiling Point Estimated high (due to large halogen atoms)
Melting Point Unknown (but affected by molecular structure)
Density Higher than water (organic compound with heavy halogens)
Solubility In Water Low (non - polar aromatic compound)
Solubility In Organic Solvents Good (e.g., in hexane, toluene etc., as it is non - polar)
Vapor Pressure Low (due to relatively high molecular weight and non - volatile nature)
Packing & Storage
Packing 100g of 2 - bromo - 5 - iodo - 1,3 - dimethylbenzene packaged in a sealed glass bottle.
Storage 2 - bromo - 5 - iodo - 1,3 - dimethylbenzene should be stored in a cool, dry, well - ventilated area. Keep it away from heat sources, flames, and oxidizing agents. Store in a tightly - sealed container, preferably made of glass or a suitable plastic, to prevent leakage and vapor escape. Label the container clearly with its name, hazards, and storage conditions.
Shipping 2 - bromo - 5 - iodo - 1,3 - dimethylbenzene is shipped in sealed, corrosion - resistant containers. Adequate cushioning is used to prevent breakage. Shipment follows strict hazardous chemical regulations to ensure safe transport.
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2-bromo-5-iodo-1,3-dimethylbenzene 2-bromo-5-iodo-1,3-dimethylbenzene 2-bromo-5-iodo-1,3-dimethylbenzene
General Information
Frequently Asked Questions
What are the physical properties of 2-bromo-5-iodine-1,3-dimethylbenzene?
The physical properties of 2-% ether-5-question-1,3-dialkylnaphthalene are as follows:
Dialkylnaphthalene is a class of organic compounds obtained by the substitution of hydrogen atoms in the naphthalene ring by alkyl groups. Its physical properties are rich and diverse, and are affected by the type, number and location of alkyl groups.
The melting point and boiling point are discussed first. Generally speaking, due to the introduction of alkyl groups, the intermolecular force changes. When the alkyl carbon chain increases or the branching chain increases, the intermolecular van der Waals force increases, resulting in an increase in the melting point and boiling point. For example, 2,6-dimethylnaphthalene, its melting point is about 112 ° C, and its boiling point is about 265 ° C.
In terms of solubility, dialkylnaphthalene is a non-polar or weakly polar molecule, so it has better solubility in non-polar or weakly polar organic solvents, such as benzene, toluene, hexane, etc.; while in polar solvents, such as water, the solubility is extremely low, because it is difficult to form effective interactions with water molecules.
In terms of density, the density of dialkylnaphthalene is usually less than that of water, and it floats on the water surface. And with the increase of alkyl carbon chain, the density tends to increase to a certain extent.
Appearance is usually colorless to light yellow liquid or solid, depending on its melting point and temperature. At room temperature, isomers with low melting point are liquid, and those with high melting point are solid.
In addition, dialkylnaphthalene has a certain degree of volatility, but its degree of volatility varies depending on the specific structure. Volatility is closely related to the intermolecular force and boiling point. The lower the boiling point and the smaller the intermolecular force, the stronger the volatility.
In practical applications, these physical properties of dialkylnaphthalene are crucial. For example, its solubility determines the choice of solvents in various chemical reactions and industrial production; melting point and boiling point affect its separation, purification and storage conditions; density is related to its location in the mixture and separation method. Understanding these physical properties is of great significance to the chemical research, industrial production and practical application of dialkylnaphthalene.
What are the chemical properties of 2-bromo-5-iodine-1,3-dimethylbenzene?
2-Alkane-5-alkyne-1,3-dimethylbenzene organic compound, having the following chemical properties:
1. ** Addition reaction **: Addition can occur due to the carbon-containing carbon triple bond and the benzene ring. The carbon-carbon triple bond can be added to hydrogen, halogen, hydrogen halide, etc. Under the action of a catalyst, it is added to hydrogen to form a carbon-carbon double bond product, and continues to hydrogenate to obtain saturated hydrocarbons. For example, under the action of Lindela catalyst, it is added with hydrogen to generate 2-alkane-5-ene-1,3-dimethylbenzene; when added with bromine water, bromine atoms are added to both ends of the carbon-carbon triple bond to fade the bromine water and use it for alkyne identification.
2. ** Oxidation reaction **: The carbon-carbon triple bond can be oxidized by a strong oxidant such as potassium permanganate. According to the reaction conditions and the position of the triple bond, the product is different, and carboxylic acids or carbon dioxide are often formed. Although the benzene ring is stable, it can also be oxidized under special conditions and strong oxidants, and the side chain methyl can be oxidized to carboxyl groups. In the case of hot acidic potassium permanganate solution, methyl groups can be oxidized to carboxyl groups to obtain aromatic compounds containing carboxyl groups. < br ** Substitution Reaction **: The benzene ring has the characteristics of substitution reaction, and the hydrogen atom on the ring can be replaced by a variety of groups. Common such as halogenation reaction, under the catalysis of iron or iron salt, reacts with halogen elemental matter, and the halogen atom replaces the hydrogen on the benzene ring; Nitrification reaction, under the action of concentrated sulfuric acid and concentrated nitric acid mixed acid, the hydrogen on the benzene ring is replaced by a nitro group; Sulfonation reaction, co-heating with concentrated sulfuric acid, and the hydrogen on the benzene ring is replaced by a sulfonic acid group.
4. ** Polymerization reaction **: contains carbon-carbon three bonds, and under certain conditions, a polymerization reaction can occur to form a polymer compound. This property is of
What is the synthesis method of 2-bromo-5-iodine-1,3-dimethylbenzene?
The synthesis of 2-% heptyl-5-alkyne-1,3-dimethylbenzene is a subject of considerable interest in organic synthetic chemistry. To obtain this compound, it can be achieved in many ways, and one of the methods is described in detail below.
First, the appropriate substituted benzene is used as the starting material. A benzene derivative containing a specific substituent is selected, and the properties and position of this substituent have a great impact on the subsequent reaction process and product structure. Here, benzene compounds with active check points and easy introduction of other groups, such as a specific halobenzene, are selected, and the halogen atom can provide an opportunity for subsequent nucleophilic substitution reactions.
Subsequently, the nucleophilic substitution reaction is used to introduce the fragment containing the alkynyl group. Under the condition of strong bases, halogenated benzene and alkynyl anions can undergo nucleophilic substitution. The preparation of alkynyl anions is often obtained by reacting the corresponding alkynes with strong bases such as sodium amide. In this step, it is crucial to precisely control the reaction conditions, such as temperature, reaction time and the proportion of reactants. If the temperature is too high, it is easy to initiate side reactions and reduce the purity of the product; if the time is too short, the reaction is incomplete and the yield is impaired.
Next, a methylation reaction is carried out to introduce dimethyl. Commonly used methylating agents such as iodomethane react with precursor compounds in the presence of suitable bases and catalysts. The alkali can be selected from potassium carbonate, etc. Its function is to capture the hydrogen atom at a specific location in the substrate molecule and make it a nucleophilic center, which then undergoes nucleophilic substitution with iodomethane, and successfully introduces methyl.
In the whole synthesis process, after each step of the reaction, it is necessary to use separation and purification methods such as column chromatography and recrystallization to ensure the purity of the intermediate product and lay a good foundation for the subsequent reaction. And for each step of the product, spectroscopy and other methods, such as nuclear magnetic resonance (NMR) and mass spectrometry (MS), should be used to accurately identify its structure and purity to ensure that the synthesis route is advanced in the expected direction, and the final target product is 2-% heptyl-5-alkyne-1,3-dimethylbenzene. In this way, the effective synthesis of this compound can be achieved by carefully designed and strictly operated synthesis steps.
In which fields is 2-bromo-5-iodine-1,3-dimethylbenzene used?
2-% arsenic-5-phosphorus-1,3-dimethylnaphthalene, although this chemical substance is not directly mentioned in the scope of Tiangongkai, it has been used in many fields in later generations.
In the field of medicine, organoarsenic compounds have been used in the treatment of syphilis and other diseases in history. Although their use is limited due to side effects and other issues, arsenic-related drug research continues. For example, arsenic-containing anti-tumor drugs have been continuously improved and optimized to provide new ways to overcome difficult diseases such as cancer. Phosphorus and its compounds are also crucial in drug synthesis. They are key elements that constitute biomacromolecules such as nucleic acids and phospholipids, and are of great significance for life-sustaining activities and the development of new drugs. Dimethylnaphthalene can be used as an important organic synthesis intermediate in drug research and development to help synthesize drug molecules with specific physiological activities.
In terms of material science, phosphorus compounds can be used to prepare materials with special properties, such as flame retardant materials. With the special reaction of phosphorus during combustion, it can effectively prevent the material from burning and spreading, and is widely used in construction, electronics and other industries with high fire protection requirements. Dimethylnaphthalene can be used to synthesize high-performance polymer materials, such as polyethylene naphthalate (PEN). Compared with common polyester materials, it has better heat resistance, mechanical properties and gas barrier properties, and has broad application prospects in packaging, electronic devices and other fields.
In the agricultural field, phosphorus-containing fertilizers are key agricultural materials to ensure crop yield and quality. Phosphorus is indispensable for the growth and development of crops, photosynthesis, energy metabolism and other processes, and can promote the development of crop root systems and improve stress resistance. Arsenic has been used as a pesticide in the form of some arsenides in the past, but its use is now strictly limited due to environmental toxicity issues. However, the research and development of new agricultural products with low toxicity and high efficiency and arsenic-related elements is still ongoing, aiming to balance the relationship between pest control and environmental protection.
What are the precautions in the preparation of 2-bromo-5-iodine-1,3-dimethylbenzene?
In the process of preparing 2-5-chloro-1,3-dimethylbenzene, more attention needs to be paid to.
First, the quality of the raw material is of paramount importance. The starting material used must be high-quality. If the raw material contains high-quality, it is easy to cause an increase in side effects, which does not reduce the quality of the target material, and is more likely to affect the quality of its products. For example, if the raw material contains a small amount of high-quality, under the anti-production or anti-production, the by-production of low-quality products will be generated, which will increase the quality of high-quality products.
Secondly, the accurate control of the anti-production parts must not be lost. The degree, resistance, reaction force and the proportion of reaction materials are all factors. For example, the reaction usually needs to be performed at a specific temperature, the reaction rate is high, and the reaction rate is accelerated. However, the reaction rate is also strong; if the reaction rate is low, the reaction rate is slow, and the reaction rate may even be difficult. Another example is the proportion of the reaction material, which needs to be fed according to the ratio of the reaction rate. If a certain amount of reaction material is low, or unnecessary side effects are caused, the source wave and the reaction rate will decrease.
Furthermore, the catalyst used in the reaction should also be properly used. The catalytic rate can be changed, but the performance of different catalytic reactions is different. It is found that it can not only efficiently promote the reaction of the eye, but also inhibit the catalytic effect of the side reaction. And the dosage also needs to be precisely controlled, and more or less dosage may affect the reaction effect.
In addition, the safety of the anti-dumping process cannot be ignored. Some anti-dumping substances may be toxic and corrosive, and the operation requirements need to follow the safety procedures. Necessary anti-dumping, such as gas masks, anti-corrosive gloves, etc. The same, anti-dumping also has requirements, and it is necessary to ensure good confidentiality to prevent the leakage of harmful substances.
is the most important, and the separation of waste materials is also important. After the anti-dumping process, the resulting mixture often contains raw materials, by-products and objects that have not been reversed. It is necessary to use the separation method, such as steaming, extraction, crystallization, etc., to obtain high-quality materials. In the separation process, it is necessary to separate the materials according to the physical properties of each product, and the operation of the combined parts to achieve the best separation effect.