Chemical Formula | C7H5BrF2 |
Molecular Weight | 207.015 |
Appearance | Typically a colorless to light - yellow liquid |
Boiling Point | Approximately 190 - 195°C |
Density | Data may vary, around 1.6 - 1.7 g/cm³ |
Solubility In Water | Insoluble |
Solubility In Organic Solvents | Soluble in common organic solvents like dichloromethane, chloroform |
Flash Point | Caution, likely flammable, flash point around 70 - 80°C |
Vapor Pressure | Low vapor pressure at room temperature |
Stability | Stable under normal conditions, but reactive towards strong nucleophiles |
Chemical Formula | C7H5BrF2 |
Molecular Weight | 207.015 |
Appearance | Liquid (predicted) |
Boiling Point | 202 - 204 °C at 760 mmHg (predicted) |
Density | 1.645 g/cm³ (predicted) |
Flash Point | 80.5 °C (predicted) |
Solubility | Insoluble in water (predicted), soluble in organic solvents like ethanol, ether (predicted) |
Vapor Pressure | 0.18 mmHg at 25 °C (predicted) |
Refractive Index | 1.511 (predicted) |
Chemical Formula | C7H5BrF2 |
Molecular Weight | 207.014 g/mol |
Appearance | Typically a colorless to light - colored liquid |
Boiling Point | Approximately 190 - 200 °C (estimated) |
Density | Estimated around 1.6 - 1.7 g/cm³ |
Solubility In Water | Insoluble in water |
Solubility In Organic Solvents | Soluble in common organic solvents like dichloromethane, chloroform |
Flash Point | Caution, likely flammable, flash point to be determined experimentally |
Vapor Pressure | Low vapor pressure at room temperature |
Chemical Formula | C7H5BrF2 |
Molar Mass | 207.015 g/mol |
Appearance | Liquid (usually) |
Boiling Point | Approximately 190 - 200 °C (estimated) |
Solubility In Water | Insoluble (organic halide, non - polar) |
Solubility In Organic Solvents | Soluble in common organic solvents like dichloromethane, chloroform, toluene |
Vapor Pressure | Low at room temperature (qualitative assessment) |
What is the main use of 2- (bromomethyl) -1,3-difluorobenzene?
2-%28bromomethyl%29-1%2C3-difluorobenzene, the Chinese name is 2 - (bromomethyl) -1,3 -difluorobenzene. The use of this substance is not good, and it is often used in the field of synthesis.
One of them can be put into the synthesis.
Polymer molecules are the best, because they contain bromomethyl difluorobenzyl, they can be replaced by other molecules such as reactants, and ingeniously introduced into the molecule. With the activity of bromomethyl, the molecule is more susceptible to other functional reactions, such as the skeleton of bromomethyl, or the characteristics of difluorophenyl, which can change the properties of the molecule, such as physical properties such as lipid solubility, and improve the efficiency of the compound.
Second, it is also indispensable in the field of synthesis. It can be used as a raw material for the synthesis of new types of biological materials, and it can be used in a reasonable and reverse way to synthesize molecules with specific biological activities. For example, bromomethyl can form active functional compounds, while difluorophenyl may increase the resistance of specific target organisms, improve the resistance of bacteria, weed control, antibacterial and other effects, and due to the introduction of fluorine atoms, it may improve the durability and biodegradability of the environment and reduce the adverse effects of the environment.
Third, it also has its application in the field of materials science. It can be introduced into polymer materials by means of polymerization and reverse reaction. Difluorophenyl can enhance the resistance and chemical properties of materials, and bromomethyl can be used as an anti-reactive agent for cross-reactive or one-step functional modification, so as to improve the special properties of materials, such as improving the mechanical properties and mechanical properties of materials, etc., and meet the needs of special material properties in different fields.
What are the physical properties of 2- (bromomethyl) -1,3-difluorobenzene
2-%28bromomethyl%29-1%2C3-difluorobenzene is 2- (bromomethyl) -1,3 -difluorobenzene, which is an organic compound. Its physical properties are as follows:
Looking at its morphology, under room temperature and pressure, it is mostly a colorless to light yellow liquid. This is determined by its molecular structure. The specific structure of carbon atoms and bromine atoms, fluorine atoms and methyl groups gives it such appearance characteristics.
Smell its smell, which has a special aromatic smell. This is due to the aromatic nature of the benzene ring structure, and the substitution of bromomethyl and fluorine atoms makes its smell unique. < Br >
Measure its boiling point, because the intermolecular force includes van der Waals force, and the presence of bromine atoms and fluorine atoms enhances the molecular polarity, causing the intermolecular force to increase, so the boiling point is relatively high, about 190-200 ℃.
Measure its melting point, affected by the regularity of molecular structure and the intermolecular force, the melting point is about -10-0 ℃, which indicates that at lower temperatures, the molecular arrangement changes from disorder to order, forming a solid lattice structure.
Looking at its solubility, since it is an organic compound, it follows the principle of "similar miscibility" and can be soluble in common organic solvents, such as ethanol, ether, dichloromethane, etc. However, due to its polar bromine atoms and fluorine atoms, their solubility in water is poor and only slightly soluble.
The density of bromine atoms is greater than that of water, which is about 1.6-1.7 g/cm ³. Due to the large weight of bromine atoms relative to atoms, the molecular weight increases. Under the same volume, the mass is greater, and the density is then greater than that of water.
Looking at its volatility, although it is not very volatile, it will evaporate into the air to a certain extent due to the thermal movement of molecules in the liquid state. In a poorly ventilated environment, its vapor concentration may increase.
The above physical properties are all determined by the molecular structure of 2 - (bromomethyl) -1,3 -difluorobenzene, and have a great impact on its application in the fields of organic synthesis and medicinal chemistry.
What is the chemical synthesis method of 2- (bromomethyl) -1,3-difluorobenzene?
To prepare 2 - (bromomethyl) -1,3 - difluorobenzene, you can follow the following method.
Take 1, 3 - difluorobenzene as the starting material. 1,3 - difluorobenzene, polyformaldehyde, hydrobromic acid and concentrated sulfuric acid are co-placed in a reaction kettle with zinc salt as the catalyst, heated to a certain temperature, so that chloromethylation occurs. This reaction process is the depolymerization of polyformaldehyde under acid catalysis to formaldehyde, formaldehyde interacts with hydrobromic acid to form bromomethanol, and 1,3 - difluorobenzene undergoes electrophilic substitution, and bromomethyl is introduced into the 2 - position of the benzene ring to generate 2 - (methyl bromide) -1,3 - difluorobenzene. However, the reaction requires fine regulation of the temperature and the ratio of reactants. If the temperature is too high, it is easy to cause the formation of multiple substitution by-products, and the improper ratio also affects the yield.
Another feasible method is to use 1,3-difluorotoluene as the raw material. First dissolve 1,3-difluorotoluene in an appropriate organic solvent, such as carbon tetrachloride, add an appropriate amount of N-bromosuccinimide (NBS), and use benzoyl peroxide as the initiator to react under light or heating conditions. NBS is the bromine source in this reaction, and under the action of the initiator, a bromine radical is generated, which captures the hydrogen atom on the 1,3-difluorotoluene methyl group, and then generates 2- (bromomethyl) -1,3-difluorobenzene. The advantage of this approach is that the reaction conditions are relatively mild, the selectivity is good, and there are few side reactions. However, it is necessary to pay attention to the amount of NBS and the reaction time. Excessive NBS or too long reaction time may lead to excessive bromination and the formation of by-products such as dibromogens.
After the reaction is completed, a post-treatment process is required. The acid and water-soluble impurities can be removed by washing with water, and then the product can be extracted with an organic solvent. The organic phase is dried with anhydrous sodium sulfate, and finally the organic solvent is removed by vacuum distillation and the product is purified to obtain pure 2- (bromomethyl) -1,3-difluorobenzene.
2- (bromomethyl) -1,3-difluorobenzene What are the precautions during storage and transportation?
2-%28bromomethyl%29-1%2C3-difluorobenzene is 2- (bromomethyl) -1,3-difluorobenzene. Many things need to be paid attention to when storing and transporting this substance.
The first priority is safety, because it is potentially dangerous. Bromomethyl is highly active, and it is easy to cause violent reactions when exposed to heat, open flames or oxidants, and even cause explosion. Therefore, when storing, be sure to store it in a cool and well-ventilated place, away from fires and heat sources, and store it separately from oxidants, acids, and bases. Do not store it together. The warehouse should have suitable materials to contain leaks.
Ensure safety during transportation. Follow relevant regulations on the transportation of hazardous chemicals and pack it properly to prevent leakage. Transportation vehicles should be equipped with corresponding fire equipment and leakage emergency treatment equipment. When driving, it should be protected from exposure to the sun, rain and high temperature. When loading and unloading, it should be handled lightly to avoid damage to packaging and containers.
Furthermore, 2- (bromomethyl) -1,3-difluorobenzene may be harmful to the environment, and it must not be allowed to enter the environment during storage and transportation. In the event of a leak, measures should be taken promptly to isolate the leaked contaminated area and restrict personnel from entering and leaving. Emergency responders should wear full masks and anti-toxic clothing to avoid contact between leaks and combustible substances. Small leaks can be absorbed by inert materials such as sand and vermiculite. Large leaks need to be built embankments or dug for containment, and transferred to a tanker or a special collector for recycling or transportation to a waste treatment site for disposal.
In summary, when storing and transporting 2- (bromomethyl) -1,3-difluorobenzene, safety is essential. Strictly follow regulations, and make protection and emergency preparations to prevent accidents and protect the environment and personnel.
What are the potential hazards of 2- (bromomethyl) -1,3-difluorobenzene to the environment and human body?
2-%28bromomethyl%29-1%2C3-difluorobenzene is 2- (bromomethyl) -1,3-difluorobenzene, which is potentially harmful to the environment and human body.
For the environment, in the soil, due to its certain chemical stability, the degradation is quite slow, or it will remain for a long time, causing adverse effects on the soil ecosystem, destroying the structure and function of soil microbial community, and hindering plant growth. In water bodies, it will cause water pollution, poison aquatic organisms, affect their survival, reproduction and development, and even change the biodiversity of aquatic ecosystems. Although the volatility in the atmosphere is limited, it will diffuse and migrate, or participate in photochemical reactions, generating secondary pollutants, which will affect air quality.
As far as human harm is concerned, it is irritating. Once it comes into contact with the skin, it can cause skin redness, swelling, pain and allergic reactions. If it comes into contact with the eyes, it will cause strong irritation to the eyes, damage the eye tissue, and cause vision loss in severe cases. Inhalation of its volatile gases can irritate the respiratory tract, causing symptoms such as cough, asthma and breathing difficulties. Long-term inhalation may damage lung function. If ingested carelessly, it will cause corrosion and toxicity to the digestive system, nausea, vomiting, abdominal pain and diarrhea, and even life-threatening conditions. In addition, based on its chemical structure and related studies, it may have certain potential carcinogenicity and teratogenicity. Long-term exposure or increase the risk of cancer may also have adverse effects on fetal development.